The c.859G>C variant in the SMN2 gene is associated with types II and III SMA and originates from a common ancestor-Reference-Cited by-同舟云学术

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The c.859G>C variant in the SMN2 gene is associated with types II and III SMA and originates from a common ancestor

Published:2010-06-24 Issue:9 Volume:47 Page:640-642
ISSN:0022-2593
Container-title:Journal of Medical Genetics
language:en
Short-container-title:Journal of Medical Genetics

Author:

Bernal S.,Alias L.,Barcelo M. J.,Also-Rallo E.,Martinez-Hernandez R.,Gamez J.,Guillen-Navarro E.,Rosell J.,Hernando I.,Rodriguez-Alvarez F. J.,Borrego S.,Millan J. M.,Hernandez-Chico C.,Baiget M.,Fuentes-Prior P.,Tizzano E. F.

Publisher

BMJ

Subject

Genetics (clinical),Genetics

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