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O.23 A novel desmin mutation causes autosomal recessive limb girdle muscular dystrophy without features of myofibrillar myopathy

✍ Scribed by Cetin, N.; Balci-Hayta, B.; Gundesli, H.; Korkusuz, P.; Purali, N.; Talim, B.; Tan, E.; Selcen, D.; Erdem-Ozdamar, S.; Dincer, P.

Book ID: 123382449
Publisher: Elsevier Science
Year: 2013
Tongue: English
Weight: 55 KB
Volume: 23
Category: Article
ISSN: 0960-8966
DOI: 10.1016/j.nmd.2013.06.733

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