Chapter 31 Immunopathology and molecular genetics of dystrophinopathies
- 1 January 2004
- book chapter
- Published by Elsevier in Supplements to Clinical Neurophysiology
- Vol. 57, 313-321
- https://doi.org/10.1016/s1567-424x(09)70367-8
Abstract
No abstract availableKeywords
This publication has 35 references indexed in Scilit:
- Muscular dystrophies involving the dystrophin–glycoprotein complex: an overview of current mouse modelsCurrent Opinion in Genetics & Development, 2002
- Function and Genetics of Dystrophin and Dystrophin-Related Proteins in MusclePhysiological Reviews, 2002
- The gene for a novel glycosyltransferase is mutated in congenital muscular dystrophy MDC1C and limb girdle muscular dystrophy 2INeuromuscular Disorders, 2002
- Caveolin‐3 is not an integral component of the dystrophin glycoprotein complexFEBS Letters, 1998
- Selective loss of sarcolemmal nitric oxide synthase in Becker muscular dystrophy.The Journal of Experimental Medicine, 1996
- Nitric oxide synthase complexed with dystrophin and absent from skeletal muscle sarcolemma in Duchenne muscular dystrophyCell, 1995
- Three muscular dystrophies: Loss of cytoskeleton-extracellular matrix linkageCell, 1995
- Syntrophin binds to an alternatively spliced exon of dystrophin.The Journal of cell biology, 1995
- Dystrophin-related protein, utrophin, in normal and dystrophic human fetal skeletal muscleJournal of Molecular Histology, 1993
- Characterisation of dystrophin in carriers of Duchenne muscular dystrophyJournal of the Neurological Sciences, 1991