Watts, Giles D J <br/><br/>
Clinical and genetic heterogeneity in chromosome 9p associated hereditary inclusion body myopathy: exclusion of GNE and three other candidate genes.  [electronic resource] 

 -  Neuromuscular disorders : NMD  Sep 2003 
 - 559-67 p.  digital 
<br/><br/> Publication Type: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0960-8966 
<br/><br/><label>Standard No.: </label>10.1016/s0960-8966(03)00070-1  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Aged<br/>Amino Acid Sequence<br/>Base Sequence<br/>Caenorhabditis elegans Proteins<br/>Carbohydrate Epimerases--genetics<br/>Carrier Proteins--genetics<br/>Chromosomes, Human, Pair 9<br/>DNA Mutational Analysis--methods<br/>DNA, Recombinant<br/>Dementia--complications<br/>Exons<br/>Genetic Heterogeneity<br/>Genetic Linkage<br/>Genetic Markers<br/>Humans<br/>Middle Aged<br/>Molecular Sequence Data<br/>Muscular Dystrophies--complications<br/>Mutation<br/>Myositis, Inclusion Body--complications<br/>NADH, NADPH Oxidoreductases--genetics<br/>Nuclear Proteins--genetics<br/>Osteitis Deformans--complications<br/>Pedigree<br/>Phosphotransferases (Alcohol Group Acceptor)--genetics<br/>RNA, Messenger--biosynthesis<br/>Reverse Transcriptase Polymerase Chain Reaction--methods<br/>Tropomyosin--genetics