Assignment of a Form of Congenital Muscular Dystrophy with Secondary Merosin Deficiency to Chromosome 1q42
- 1 February 2000
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 66 (2) , 428-435
- https://doi.org/10.1086/302775
Abstract
No abstract availableKeywords
This publication has 32 references indexed in Scilit:
- Distribution of emerin and lamins in the heart and implications for Emery-Dreifuss muscular dystrophyHuman Molecular Genetics, 1999
- Assignment of the Muscle-Eye-Brain Disease Gene to 1p32-p34 by Linkage Analysis and Homozygosity MappingAmerican Journal of Human Genetics, 1999
- Laminin α2-chain gene mutations in two siblings presenting with limb-girdle muscular dystrophyNeuromuscular Disorders, 1998
- Identification of a New Locus for a Peculiar Form of Congenital Muscular Dystrophy with Early Rigidity of the Spine, on Chromosome 1p35-36American Journal of Human Genetics, 1998
- Variable clinical phenotype in merosin-deficient congenital muscular dystrophy associated with differential immunolabelling of two fragments of the laminin α2 chainNeuromuscular Disorders, 1997
- Muscle—eye—brain disease: A neuropathological studyAnnals of Neurology, 1997
- Mild clinical phenotype in a 12-year-old boy with partial merosin deficiency and central and peripheral nervous system abnormalitiesNeuromuscular Disorders, 1996
- Mutations in the laminin α2–chain gene (LAMA2) cause merosin–deficient congenital muscular dystrophyNature Genetics, 1995
- Localization of a gene for Fukuyama type congenital muscular dystrophy to chromosome 9q31–33Nature Genetics, 1993
- Complete cloning of the duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individualsCell, 1987