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Refined Mapping of a Gene Responsible for Fukuyama-Type Congenital Muscular Dystrophy: Evidence for Strong Linkage Disequilibrium

Fukuyama-type congenital muscular dystrophy (FCMD), the second most common form of childhood muscular dystrophy in Japan, is an autosomal recessive severe muscular dystrophy associated with an anomaly of the brain. After our initial mapping of the FCMD locus to chromosome 9q31-33, we further defined...

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Detalhes bibliográficos
Main Authors: Toda, Tatsushi, Ikegawa, Shiro, Okui, Keiko, Kondo, Eri, Saito, Kayoko, Fukuyama, Yukio, Yoshioka, Mieko, Kumagai, Toshiyuki, Suzumori, Kaoru, Kanazawa, Ichiro, Nakamura, Yusuke
Formato: Artigo
Idioma:Inglês
Publicado em: 1994
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1918318/
https://ncbi.nlm.nih.gov/pubmed/7977357
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