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Publikováno v:
Clinical Orthopaedics and Related Research. 401:88-106
The cloning of the dystrophin gene has led to major advances in the understanding of the molecular genetic basis of Duchenne, Becker, and other muscular dystrophies associated with mutations in genes encoding members of the dystrophin-associated glyc
Autor:
Paula C. Demacio, Peter N Ray
Publikováno v:
Genome. 44:990-994
Familial dysautonomia is a severe autosomal-recessive neurodegenerative disease that primarily affects the Ashkenazi Jewish population. We present the mapping of α-catulin and show that it maps precisely to the familial dysautonomia candidate region