Human Molecular Genetics · 1994 · 199 citations · 17 references
Life SciencesGeneticsMolecular GeneticsHuman GeneticsMedical GeneticsNeuromuscular DisordersChromosomal AbnormalitiesChromosomal DisordersGenetic DisordersMuscle DisordersMuscular DystrophyStructural Chromosome AbnormalitiesHomozygosity MappingLaminin BiologyMerosin-deficient Congenital Muscular DystrophyMuscular Dystrophy GeneticsStructural Brain Abnormalities
Congenital muscular dystrophies (CMD) are autosomal recessive, heterogeneous disorders. The commonest forms are the Fukuyama CMD (FCMD), associated with mental retardation and structural brain anomalies, and classical (occidental) CMD, with pure muscle expression. FCMD has been localized to chromosome 9q31-q33. Following the discovery of merosin deficiency in some CMD cases, we have localized, by homozygosity mapping and linkage analysis (Zmax = 5.6; theta = 0.0 for marker AFM127xb2) in four merosin-negative families a CMD gene in a 16 cM region of chromosome 6q2 in the region of the laminin M chain gene. In three consanguineous, merosin-positive, CMD families there was no linkage to either chromosome 6q2 or 9q31-q33.
17
Analysis of Human Genetic Linkage.
A. W. F. Edwards, J Ott · Biometrics · 1992 · 1.7K citations
A second-generation linkage map of the human genome
Jean Weissenbach, Gàbor Gyapay, Colette Dib et al. · Nature · 1992 · 1.7K citations
Membrane organization of the dystrophin-glycoprotein complex
James M. Ervasti, Kevin P. Campbell · Cell · 1991 · 1.3K citations
Multilocus linkage analysis in humans: detection of linkage and estimation of recombination.
G.M. Lathrop, J.-M. Lalouel, Cécile Julier et al. · PubMed · 1985 · 1.2K citations