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Confirmation of linkage of oculopharyngeal muscular dystrophy to chromosome 14q11.2-q13 in American families suggests the existence of a second causal mutation

American FamiliesRare DiseasesSecond Causal MutationDevelopmental BiologyMendelian DisorderGenetic DisorderGeneticsGenetic EpidemiologyMolecular GeneticsDisease Gene IdentificationOculopharyngeal Muscular DystrophyMedicineClinical Genetics