Linkage of Familial Dilated Cardiomyopathy with Conduction Defect and Muscular Dystrophy to Chromosome 6q23
- 1 October 1997
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 61 (4) , 909-917
- https://doi.org/10.1086/514896
Abstract
No abstract availableKeywords
This publication has 34 references indexed in Scilit:
- Refinement of the laminin alpha2 chain locus to human chromosome 6q2 in severe and mild merosin deficient congenital muscular dystrophy.Journal of Medical Genetics, 1997
- Merosin/laminin-2 and muscular dystrophyNeuromuscular Disorders, 1996
- Beyond dystrophinCurrent Opinion in Pediatrics, 1996
- Mapping a cardiomyopathy locus to chromosome 3p22-p25.Journal of Clinical Investigation, 1996
- Deficiency of Merosin (Laminin M or α2) in Congenital Muscular Dystrophy Associated with Cerebral White Matter AlterationsNeuropediatrics, 1995
- Mutations in the laminin α2–chain gene (LAMA2) cause merosin–deficient congenital muscular dystrophyNature Genetics, 1995
- Three muscular dystrophies: Loss of cytoskeleton-extracellular matrix linkageCell, 1995
- A gene defect that causes conduction system disease and dilated cardiomyopathy maps to chromosome 1p1–1q1Nature Genetics, 1994
- X-Linked Dilated CardiomyopathyNew England Journal of Medicine, 1987
- Muscular dystrophy in the mouse caused by an allele at the -locusLife Sciences, 1970