PABPN1 (GCN)11 as a Dominant Allele in Oculopharyngeal Muscular Dystrophy –Consequences in Clinical Diagnosis and Genetic Counselling - Archive ouverte HAL Accéder directement au contenu
Article Dans Une Revue Journal of Neuromuscular Diseases Année : 2015

PABPN1 (GCN)11 as a Dominant Allele in Oculopharyngeal Muscular Dystrophy –Consequences in Clinical Diagnosis and Genetic Counselling

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hal-03832803 , version 1 (27-10-2022)

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Pascale Richard, Capucine Trollet, Teresa Gidaro, Laurence Demay, Guy Brochier, et al.. PABPN1 (GCN)11 as a Dominant Allele in Oculopharyngeal Muscular Dystrophy –Consequences in Clinical Diagnosis and Genetic Counselling. Journal of Neuromuscular Diseases, 2015, 2 (2), pp.175-180. ⟨10.3233/JND-140060⟩. ⟨hal-03832803⟩
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