Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy
Year: 1998
Type: article
Study design: Observational Study
Source: Nature Genetics
DOI: 10.1038/ng0298-164
Authors: Bernard Brais, Jean-Pierre Bouchard, Ya-Gang Xie, Daniel L. Rochefort, Nathalie Chrétien, Fernando M.S. Tomé, Ronald G. Lafrentére, Johanna M. Rommens, Eichiro Uyama, Osamu Nohira, Segiu Blumen, Amos D. Korcyn, Peter Heutink, Jean Mathieu, André Duranceau, Francois Codère, Michel Fardeau, Guy A. Rouleau
Institutions: Montreal General Hospital, McGill University, Hôpital de l'Enfant-Jésus, Inserm, Institut de Myologie, Hospital for Sick Children, Kumamoto University, Shizuoka Red Cross Hospital, Hillel Yaffe Medical Center, Tel Aviv University, Erasmus University Rotterdam, Hôpital de Chicoutimi, Centre Hospitalier de l’Université de Montréal, Royal Victoria Hospital
Language: English
Subfield: Cellular and Molecular Neuroscience
Field: Neuroscience
Domain: Life Sciences
Open Access status: green
OpenAlex ID: W2113559242