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SETX gene mutation in a family diagnosed autosomal dominant proximal spinal muscular atrophy

✍ Scribed by Sabine Rudnik-Schöneborn; Larissa Arning; Jörg T. Epplen; Klaus Zerres

Book ID: 116795207
Publisher: Elsevier Science
Year: 2012
Tongue: English
Weight: 648 KB
Volume: 22
Category: Article
ISSN: 0960-8966
DOI: 10.1016/j.nmd.2011.09.006

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