Genetics and Congenital Deafness
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Identification Of New Genetic Deafness Syndrome
medicalnewstoday.com — “Ten years ago, scientists seeking to understand how a certain type of feature on a cell called an L-type calcium channel worked created a knockout mouse missing both copies of the CACNA1D gene.” View full resource at medicalnewstoday.com
Most Recently Shared on March 10, 2011 at 11:05 am By:
Identification Of New Genetic Deafness Syndrome http://mnt.to/3S6X #hearing #deafness
New genetic deafness syndrome identified
eurekalert.org — “Ten years ago, scientists seeking to understand how a certain type of feature on a cell called an L-type calcium channel worked created a knockout mouse missing both copies of the CACNA1D gene.” View full resource at eurekalert.org
Most Recently Shared on March 9, 2011 at 9:30 pm By:
New genetic deafness syndrome identified : http://eurekalert.org/e/3tzd
New genetic deafness syndrome identified
physorg.com — “Ten years ago, scientists seeking to understand how a certain type of feature on a cell called an L-type calcium channel worked created a knockout mouse missing both copies of the CACNA1D gene.” View full resource at physorg.com
Most Recently Shared on March 9, 2011 at 7:53 pm By:
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New genetic deafness syndrome identified http://tw.physorg.com/218901859
New Genetic Deafness Syndrome Identified
newswise.com — “Ten years ago, scientists seeking to understand how a certain type of feature on a cell called an L-type calcium channel worked created a knockout mouse missing both copies of the CACNA1D gene.” View full resource at newswise.com
Most Recently Shared on March 9, 2011 at 4:22 pm By:
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New Genetic Deafness Syndrome Identified: Ten years ago, scientists seeking to understand how a certain type of ... http://bit.ly/hykUOB
Congenital heart disease 'linked with genetic mechanism'
spirehealthcare.com — “23 January 2012 Scientists at the Gladstone Institutes have found a genetic mechanism linked directly to congenital heart disease” View full resource at spirehealthcare.com
Most Recently Shared on January 24, 2012 at 5:21 pm By:
Congenital heart disease linked to genetic mechanism. http://t.co/SCCru2U1
News: Researchers to investigate the genetics of congenital heart disease.
genengnews.com — “Children's Hospital Boston and Brigham and Women's Hospital to search for undiscovered mutations as part of national collaboration Researchers at Children's Hospital Boston and Br” View full resource at genengnews.com
Most Recently Shared on December 22, 2009 at 4:58 pm By:
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Researchers to investigate the genetics of congenital heart disease - Genetic Engineering News (press release) http://bit.ly/7aIap2
Genetic Cause For Type Of Deafness Identified By Scripps Research Scientists
medicalnewstoday.com — “A team led by scientists from The Scripps Research Institute has discovered a genetic cause of progressive hearing loss. The findings will help scientists better understand the nature of age-relat” View full resource at medicalnewstoday.com
Most Recently Shared on September 5, 2009 at 12:04 pm By:
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Genetic Cause For Type Of Deafness Identified By Scripps Research Scientists: A team led by scientists from The .. http://bit.ly/aSD8x
New Gene For Childhood Deafness Discovered
medicalnewstoday.com — “RNID funded research has discovered a new gene linked to inherited deafness, which could mean that more families will be able to identify the cause of their hearing loss. The discovery” View full resource at medicalnewstoday.com
Most Recently Shared on April 14, 2010 at 4:15 pm By:
New Gene For Childhood Deafness Discovered http://mnt.to/3Bdn #hearing #deafness
Mutated Muscle Protein Causes Deafness
medicalnewstoday.com — “Excessive noise is not the only thing that causes damage to hearing. In many cases, genetic factors are responsible for the loss of hearing at a young age. Researchers at the Max Planck Institute” View full resource at medicalnewstoday.com
Most Recently Shared on May 31, 2011 at 7:05 am By:
Mutated Muscle Protein Causes Deafness http://mnt.to/3WwK #biology
A novel DCC mutation and genetic heterogeneity in congenital mirror movements --" Neurology
neurology.org — “A novel DCC mutation and genetic heterogeneity in congenital mirror movements --" Neurology” View full resource at neurology.org
Most Recently Shared on January 20, 2011 at 4:22 pm By:
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A novel DCC mutation and genetic heterogeneity in congenital mirror movements http://bit.ly/gABpef #neurology
The genetics of heart defects | NHS Choices | Nursing Times
nursingtimes.net — “Treatments for heart defects could be improved by the identification of the gene behind the condition, says The Daily Telegraph.” View full resource at nursingtimes.net
Most Recently Shared on June 6, 2010 at 6:26 am By:
Behind the Headlines The genetics of heart defects: “Treatments for heart defects could be improved†by the identi... http://bit.ly/9w0hW6
Defining Hereditary Deafness Through Exome Sequencing
medicalnewstoday.com — “Precise diagnosis of disease and developmental syndromes often depends on understanding the genetics underlying them. Most cases of early onset hearing loss are genetic in origin but there are man” View full resource at medicalnewstoday.com
Most Recently Shared on September 16, 2011 at 7:05 am By:
Defining Hereditary Deafness Through Exome Sequencing http://mnt.to/3ZFy #genetics
How Mitochondrial DNA Defects Cause Inherited Deafness
medicalnewstoday.com — “Yale scientists have discovered the molecular pathway by which maternally inherited deafness appears to occur: Mitochondrial DNA mutations trigger a signaling cascade, resulting in programmed cell” View full resource at medicalnewstoday.com
Most Recently Shared on February 21, 2012 at 8:05 am By:
How Mitochondrial DNA Defects Cause Inherited Deafness http://t.co/DrZcbsQO #genetics
Gene Mutation Identified, Causes Rare Form Of Deafness
medicalnewstoday.com — “Researchers have identified a gene mutation that causes a rare form of hearing loss known as auditory neuropathy, according to U-M Medical School scientists.In the study published online” View full resource at medicalnewstoday.com
Most Recently Shared on July 13, 2010 at 11:56 am By:
Gene Mutation Identified, Causes Rare Form Of Deafness: Researchers have identified a gene mutation that causes a ... http://mnt.to/f/3FZD
Congenital Erythropoietic Porphyria: eMedicine Dermatology
emedicine.medscape.com — “Overview: Erythropoietic porphyria (EP) is a rare inborn error of porphyrin-heme synthesis inherited that is as an autosomal recessive trait. The inheritance of 2 mutant alleles for the gene encoding the enzyme uroporphyrinogen III synthase leads to ...” View full resource at emedicine.medscape.com
Most Recently Shared on April 21, 2010 at 12:06 am By:
Congenital erythropoietic protoporphyria is a genetic disorder involving a deficiency of the enzyme ferrochelatase. http://bit.ly/91GRwn
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