F.M.S. Tomé

Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy

Bernard Brais, Jean‐Pierre Bouchard, Ya‐Gang Xie et al. · Nature Genetics · 1998 · 798 citations · Full text

Life Sciences, Genetics, Molecular Genetics +8

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

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

Missense mutations in the adhalin gene linked to autosomal recessive muscular dystrophy

Steven L. Roberds, France Leturcq, Valérie Allamand et al. · Cell · 1994 · 457 citations

Life Sciences, Genetics, Molecular Genetics +11

Immunolocalization and developmental expression of dystrophin related protein in skeletal muscle

Tejvir S. Khurana, Simon C. Watkins, Philippe Chafey et al. · Neuromuscular Disorders · 1991 · 263 citations

Medicine, Cell Biology, Molecular Biology +14