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Lancet (London, England)|June 1, 2000
Association of nonsense mutation of dystrophin gene with disruption of sarcoglycan complex in X-linked dilated cardiomyopathyW M Franz, M Müller, O J Müller, et al.
Neuropediatrics|June 1, 1995
Preserved merosin M-chain (or laminin-alpha 2) expression in skeletal muscle distinguishes Walker-Warburg syndrome from Fukuyama muscular dystrophy and merosin-deficient congenital muscular dystrophyT Voit, C A Sewry, K Meyer, et al.
American Journal of Medical Genetics|October 27, 1998
Megalencephaly, mega corpus callosum, and complete lack of motor development: a previously undescribed syndromeG Göhlich-Ratmann, M Baethmann, P Lorenz, et al.
Neurology|January 13, 2010
Correlation of enzyme activity and clinical phenotype in POMT1-associated dystroglycanopathiesM Lommel, S Cirak, T Willer, et al.
Hepatology (Baltimore, Md.)|March 7, 2001
Morphogenesis of primary human biliary epithelial cells: induction in high-density culture or by coculture with autologous human hepatocytesM K Auth, R E Joplin, M Okamoto, et al.
FEBS Letters|April 22, 1991
A homologue of dystrophin is expressed at the neuromuscular junctions of normal individuals and DMD patients, and of normal and mdx mice. Immunological evidenceF Pons, N Augier, J O Léger, et al.
Neurology|April 11, 2001
Secondary calpain3 deficiency in 2q-linked muscular dystrophy: titin is the candidate geneH Haravuori, A Vihola, V Straub, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 17, 2005
Laing early onset distal myopathy: slow myosin defect with variable abnormalities on muscle biopsyP J Lamont, B Udd, F L Mastaglia, et al.
Genomics|January 1, 1996
A gene for autosomal dominant paroxysmal choreoathetosis/spasticity (CSE) maps to the vicinity of a potassium channel gene cluster on chromosome 1p, probably within 2 cM between D1S443 and D1S197G Auburger, T Ratzlaff, A Lunkes, et al.
Pediatric Research|September 1, 1996
Wheat kernel ingestion protects from progression of muscle weakness in mdx mice, an animal model of Duchenne muscular dystrophyC Hübner, H A Lehr, R Bodlaj, et al.
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