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C.P.2.04 Skipping of exon 16 in COL6A3 is a recurrent mutation causing severe congenital muscular dystrophy type Ullrich

✍ Scribed by Y. Zou; J. Schessl; A. Lampe; Y. Hu; C. Jiménez-Mallebrera; G. Schreiber; I. Stolte-Dijkstra; A. Fock; M. Chu; K. Bushby; R. Weiss; K. Flanigan; F. Muntoni; C. Bönnemann

Book ID: 116793129
Publisher: Elsevier Science
Year: 2007
Tongue: English
Weight: 51 KB
Volume: 17
Category: Article
ISSN: 0960-8966
DOI: 10.1016/j.nmd.2007.06.280

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