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Neurology, ISSN 0028-3878, 04/2015, Volume 84, Issue 17, pp. 1772 - 1781
OBJECTIVE:To determine the clinical spectrum of limb-girdle muscular dystrophy 2E (LGMD2E) and to investigate whether genetic or biochemical features can... 
INVOLVEMENT | CARDIOMYOPATHY | BETA-SARCOGLYCAN | ALPHA | GAMMA-SARCOGLYCAN | MUTATIONS | IDENTIFICATION | DELTA-SARCOGLYCAN | SARCOGLYCAN COMPLEX | DEFICIENCY | CLINICAL NEUROLOGY | 185
Journal Article
MOVEMENT DISORDERS, ISSN 0885-3185, 11/2016, Volume 31, Issue 11, pp. 1694 - 1703
BackgroundMyoclonus-dystonia is a neurogenic movement disorder caused by mutations in the gene encoding -sarcoglycan. By contrast, mutations in the -, -, -,... 
NERVOUS-SYSTEM | GAMMA-SARCOGLYCAN | PLASMA-MEMBRANE | CLINICAL NEUROLOGY | ALPHA-SARCOGLYCAN | sarcoglycan | ZETA-SARCOGLYCAN | dystonia | GLYCOPROTEIN COMPLEX | DYT11 | MOLECULAR PATHOGENESIS | PSYCHIATRIC-DISORDERS | BETA-SARCOGLYCAN | DELTA-SARCOGLYCAN
Journal Article
Journal Article
by Li, DJ and Yue, YP and Lai, Y and Hakim, CH and Duan, DS
JOURNAL OF PATHOLOGY, ISSN 0022-3417, 01/2011, Volume 223, Issue 1, pp. 88 - 98
The mechanism of force reduction is not completely understood in Duchenne muscular dystrophy (DMD), a dystrophin-deficient lethal disease. Nitric oxide... 
mdx | ryanodine receptor 1 | delta-sarcoglycan | OXIDATIVE STRESS | NITRIC-OXIDE SYNTHASE | CONTRACTION-INDUCED INJURY | DEFICIENT SKELETAL-MUSCLE | dystrophin | PATHOLOGY | MDX MICE | nitrosative stress | ONCOLOGY | nitrotyrosination | RYANODINE RECEPTOR | Duchenne muscular dystrophy | nNOS | S-nitrosylation | L-ARGININE | GLYCOPROTEIN COMPLEX | DUCHENNE MUSCULAR-DYSTROPHY | mdx4cv
Journal Article
Journal Article
Journal Article