Stensland, Eva <br/><br/>
Prevalence, mutation spectrum and phenotypic variability in Norwegian patients with Limb Girdle Muscular Dystrophy 2I.  [electronic resource] 

 -  Neuromuscular disorders : NMD  Jan 2011 
 - 41-6 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1873-2364 
<br/><br/><label>Standard No.: </label>10.1016/j.nmd.2010.08.008  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Age of Onset<br/>Family Health<br/>Female<br/>Genetic Association Studies<br/>Humans<br/>Longitudinal Studies<br/>Male<br/>Middle Aged<br/>Muscular Dystrophies, Limb-Girdle--epidemiology<br/>Mutation--genetics<br/>Norway--epidemiology<br/>Pentosyltransferases<br/>Phenotype<br/>Prevalence<br/>Proteins--genetics<br/>Retrospective Studies<br/>Young Adult