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Autor:
Canki-Klain, Nina, Šoštarko, Marija, Vranješ, Davorka, Urtizberea Jan Andoni 2 Richard Pascale, Zurak, Niksa
Oculopharyngeal musular dystrophy (OPMD) (MIM 164 300) is an autosomal dominant generalised myopathy caused by short (GCG)8-13 coding triplet repeat expansions in the polyadenylation binding protein 2 (PABP2) gene. First described in French Canadians
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::cc18611fd8c1391d28197e313425a37b
https://www.bib.irb.hr/70010
https://www.bib.irb.hr/70010
