New POMT2 mutations causing congenital muscular dystrophy: Identification of a founder mutation-Reference-Cited by-同舟云学术

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New POMT2 mutations causing congenital muscular dystrophy: Identification of a founder mutation

Published:2007-07-18 Issue:12 Volume:69 Page:1254-1260
ISSN:0028-3878
Container-title:Neurology
language:en
Short-container-title:Neurology

Author:

Yanagisawa A.,Bouchet C.,Van den Bergh P.Y.K.,Cuisset J. -M.,Viollet L.,Leturcq F.,Romero N. B.,Quijano-Roy S.,Fardeau M.,Seta N.,Guicheney P.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical)

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