Relative frequency of congenital muscular dystrophy subtypes: Analysis of the UK diagnostic service 2001–2008

Mutations in the laminin α2–chain gene (LAMA2) cause merosin–deficient congenital muscular dystrophy

A. Leclerc, Xu Zhang, Haluk Topaloğlu et al. · Nature Genetics · 1995 · 628 citations

Life Sciences, Genetics, Molecular Genetics +9

Prevalence of genetic muscle disease in Northern England: in-depth analysis of a muscle clinic population

Fiona Norwood, Chris Harling, Patrick F. Chinnery et al. · Brain · 2009 · 533 citations · Full text

Medicine, Genetics, Pathology +11

Congenital muscular dystrophy with merosin deficiency.

F.M.S. Tomé, Teresinha Evangelista, A. Leclerc et al. · PubMed · 1994 · 459 citations

Medicine, Molecular Biology, Pathology +17

Refining genotype phenotype correlations in muscular dystrophies with defective glycosylation of dystroglycan

C. Godfrey, Emma Clement, R. Mein et al. · Brain · 2007 · 440 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Mutations in the integrin α7 gene cause congenital myopathy

Yukiko Hayashi, Fan-Li Chou, Eva Engvall et al. · Nature Genetics · 1998 · 358 citations

Life Sciences, Genetics, Molecular Genetics +7