Oculopharyngodistal myopathy is genetically heterogeneous and most cases are distinct from oculopharyngeal muscular dystrophy

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

Oculopharyngeal Muscular Dystrophy

Bernard Brais, Guy A. Rouleau, Jean-Pierre Bouchard et al. · Seminars in Neurology · 1999 · 178 citations

Medicine, Genetics, Molecular Genetics +16

The oculopharyngeal muscular dystrophy locus maps to the region of the cardiac α and β myosin heavy chain genes on chromosome 14q11.2−q13

Bernard Brais, Ya‐Gang Xie, Marc Sanson et al. · Human Molecular Genetics · 1995 · 150 citations

Life Sciences, Genetics, Molecular Genetics +12

Oculopharyngodistal Myopathy

E Satoyoshi · Archives of Neurology · 1977 · 119 citations

Medicine, Neurology, Pathology +8

Morphological changes in muscle fibers in oculopharyngeal muscular dystrophy

F.M.S. Tomé, Danielle Château, A. Leclerc et al. · Neuromuscular Disorders · 1997 · 111 citations

Medicine, Anatomy, Neurology +16