Human Genome Epidemiology Literature Finder
Rare Diseases
Records 1 - 3 (of 3 Records) |
Query Trace: Oculopharyngeal Muscular Dystrophy[original query] |
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Oculopharyngeal muscular dystrophy: phenotypic and genotypic studies in a UK population. Brain : a journal of neurology 2001 Mar 124 (Pt 3): 522-6. Hill M E, Creed G A, McMullan T F, Tyers A G, Hilton-Jones D, Robinson D O, Hammans S |
[Haplotype Analysis of Oculopharyngeal Muscular Dystrophy (OPMD) Locus in Yakutia]. Genetika 2016 Mar 52 (3): 376-84. Marusin A V, Kurtanov Kh A, Maksimova N R, Svarovskaya M G, Stepanov V |
Characterization of PABPN1 expansion mutations in a large cohort of Mexican patients with oculopharyngeal muscular dystrophy (OPMD). Journal of investigative medicine : the official publication of the American Federation for Clinical Research 2016 Dec . Cruz-Aguilar Marisa, Guerrero-de Ferran Caroline, Tovilla-Canales Jose Luis, Nava-Castañeda Angel, Zenteno Juan |
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