Author:
Fischmann Arne,Gloor Monika,Fasler Susanne,Haas Tanja,Rodoni Wetzel Rachele,Bieri Oliver,Wetzel Stephan,Heinimann Karl,Scheffler Klaus,Fischer Dirk
Publisher
Springer Science and Business Media LLC
Subject
Clinical Neurology,Neurology
Reference21 articles.
1. Semmler A, Kress W, Vielhaber S, Schröder R, Kornblum C (2007) Variability of the recessive oculopharyngeal muscular dystrophy phenotype. Muscle Nerve 35(5):681–684
2. Fan X, Rouleau GA (2003) Progress in understanding the pathogenesis of oculopharyngeal muscular dystrophy. Can J Neurol Sci 30(1):8–14
3. Barbeau A (1969) Oculopharyngeal muscular dystrophy in French Canada (abstract of the presidential address). In: Brunette JR, Barbeau A (eds) Progress in neuro-ophthalmology Vol. 2. Excerpta Medica, Amsterdam, p 3
4. Fardeau M, Tomé FM (1997) Oculopharyngeal muscular dystrophy in France. Neuromuscul Disord 7:S30–S33
5. Brais B, Bouchard JP, Xie YG, Rochefort DL, Chrétien N, Tomé FM, Lafrenière RG, Rommens JM, Uyama E, Nohira O, Blumen S, Korczyn AD, Heutink P, Mathieu J, Duranceau A, Codère F, Fardeau M, Rouleau GA, Korcyn AD (1998) Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy. Nat Genet 18(2):164–167
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