Clinical phenotype in congenital muscular dystrophy: correlation with expression of merosin in skeletal

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

Deficiency of merosin in dystrophic dy mice and genetic linkage of laminin M chain gene to dy locus.

Yoshihide Sunada, Suzanne M. Bernier, Christine A. Kozak et al. · Journal of Biological Chemistry · 1994 · 293 citations · Full text

Medicine, Genetics, Molecular Biology +17

Muscle Disorders in Childhood

Theodore L. Munsat · Neurology · 1979 · 292 citations

Medicine, Child Health, Pediatrics +7

Human laminin M chain (merosin): complete primary structure, chromosomal assignment, and expression of the M and A chain in human fetal tissues

Reetta Vuolteenaho, Marja Nissinen, Kirsi Sainio et al. · The Journal of Cell Biology · 1994 · 262 citations · Full text

Life Sciences, Biochemistry, Molecular Biology +12

Localization of merosin-negative congenital muscular dystrophy to chromosome 6q2 by homozygosity mapping

Dominique Hillaire, A. Leclerc, Sabine Fauré et al. · Human Molecular Genetics · 1994 · 199 citations

Life Sciences, Genetics, Molecular Genetics +14