Sarcolemmopathy: Muscular Dystrophies with Cell Membrane Defects
Author:
Publisher
Wiley
Subject
Neurology (clinical),Pathology and Forensic Medicine,General Neuroscience
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1750-3639.2001.tb00394.x/fullpdf
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2. A gene related to Caenorhabditis elegans spermatogenesis factor fer-1 is mutated in limb-girdle muscular dystrophy type 2B;Bashir;Nature Genetics,1998
3. Eine neue x-chromosomale Muskeldystrophie;Becker;Arch Psychiatr Z Neurol,1955
4. Severe childhood muscular dystrophy affecting both sexes and frequent in Tunisia;Hamida;Muscle Nerve,1983
5. Benign myopathy, with autosomal dominant inheritance. A report on three pedigrees;Bethlem;Brain,1976
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