Oculopharyngeal muscular dystrophy
Author:
Publisher
Oxford University Press (OUP)
Subject
Clinical Neurology
Link
http://academic.oup.com/brain/article-pdf/124/3/522/17873176/1240522.pdf
Reference15 articles.
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2. Coquet M, Vital C, Julien J. Presence of inclusion body myositis-like filaments in oculopharyngeal muscular dystrophy. Ultrastructural study of 10 cases. Neuropathol Appl Neurobiol1990; 16: 393–400.
3. Fried K, Arlozorov A, Spira R. Autosomal recessive oculopharyngeal muscular dystrophy. J Med Genet1975; 12: 416–8.
4. Grewal RP, Cantor R, Turner G, Grewal RK, Detera-Wadleigh SD. Genetic mapping and haplotype analysis of oculopharyngeal muscular dystrophy. Neuroreport1998; 9: 961–5.
5. Grewal RP, Karkera JD, Grewal RK, Detera-Wadleigh SD. Mutation analysis of oculopharyngeal muscular dystrophy in Hispanic American families. Arch Neurol1999; 56: 1378–81.
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