Nemaline Myopathy
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Research finds alteration in KBTBD13 protein causes nemaline myopathy
news-medical.net — “Researchers from the Department of Anesthesiology, Uniformed Services University of the Health Sciences (USU), along with research teams from the National Institutes of Health and from Australia, the Netherlands and Spain, have identified a novel gene on chromosome 15q that, when altered, causes nemaline myopathy with cores, a rare inherited muscle disorder. The gene encodes a member of the BTB/Kelch family of proteins.” View full resource at news-medical.net
Most Recently Shared on November 30, 2010 at 8:29 am By:
Research finds alteration in KBTBD13 protein causes nemaline myopathy: Researchers from the Department of Anesth... http://bit.ly/h29TPs
New avenue for treating myopathy - News
virtualmedicalcentre.com — “West Australian Institute of Medical Research (WAIMR) scientists have rewritten the book on nemaline myopathy, a type of congenital myopathy that can cause death or paralysis in newborn babies.” View full resource at virtualmedicalcentre.com
Most Recently Shared on June 9, 2011 at 2:07 pm By:
VirtualMedicalCentre Health Site
New avenue for treating myopathy http://dlvr.it/VgnC7 #Healthnews
Researchers Identify Novel Gene Connected To Rare Muscle Disease
medicalnewstoday.com — “Researchers from the Department of Anesthesiology, Uniformed Services University of the Health Sciences (USU), along with research teams from the National Institutes of Health and from Australia,” View full resource at medicalnewstoday.com
Most Recently Shared on November 30, 2010 at 2:05 pm By:
MNT - Muscular Dys Health News
Researchers Identify Novel Gene Connected To Rare Muscle Disease http://mnt.to/3Nh7 #musculardystrophy
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