Disruption of the β-Sarcoglycan Gene Reveals Pathogenetic Complexity of Limb-Girdle Muscular Dystrophy Type 2E
- 1 January 2000
- journal article
- research article
- Published by Elsevier in Molecular Cell
- Vol. 5 (1), 141-151
- https://doi.org/10.1016/s1097-2765(00)80410-4
Abstract
No abstract availableKeywords
This publication has 45 references indexed in Scilit:
- Membrane Targeting and Stabilization of Sarcospan Is Mediated by the Sarcoglycan SubcomplexThe Journal of cell biology, 1999
- LGMD 2E in Tunisia is caused by a homozygous missense mutation in β-sarcoglycan exon 3Neuromuscular Disorders, 1998
- Functional Rescue of the Sarcoglycan Complex in the BIO 14.6 Hamster Using δ-Sarcoglycan Gene TransferMolecular Cell, 1998
- β-Sarcoglycan: genomic analysis and identification of a novel missense mutation in the LGMD2E Amish isolateNeuromuscular Disorders, 1998
- Human ϵ‐sarcoglycan is highly related to α‐sarcoglycan (adhalin), the limb girdle muscular dystrophy 2D gene1FEBS Letters, 1998
- Mouse Adhalin: Primary Structure and Expression during Late Stages of Muscle Differentiationin VitroBiochemical and Biophysical Research Communications, 1997
- Expression of Escherichia coli β-Galactosidase and Rat HPRT in the CNS of Macaca mulatta Following Adenoviral Mediated Gene TransferExperimental Neurology, 1994
- Localization of dystrophin gene transcripts during mouse embryogenesis.The Journal of cell biology, 1992
- Gastric Hypomotility in Duchenne's Muscular DystrophyNew England Journal of Medicine, 1988
- Microvascular spasm in the cardiomyopathic Syrian hamster: a preventable cause of focal myocardial necrosis.Circulation, 1982