Two cases of oculopharyngeal muscular dystrophy (OPMD) with...

Neuromuscular Disorders 2011 Vol. 21; Iss. 11

Two cases of oculopharyngeal muscular dystrophy (OPMD) with the rare PABPN1 c.35G > C; p.Gly12Ala point mutation

David O. Robinson, David Hilton-Jones, David Mansfield, Göran Darius Hildebrand, Sophie Marks, Dorothy Mechan, Joanne Ramsay
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Volume:
21
Year:
2011
Language:
english
DOI:
10.1016/j.nmd.2011.06.003
File:
PDF, 306 KB
english, 2011
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