Mutations in KLHL40 Are a Frequent Cause of Severe Autosomal-Recessive Nemaline Myopathy
Ravenscroft, Gianina, Miyatake, Satoko, Lehtokari, Vilma-Lotta, Todd, Emily J., Vornanen, Pauliina, Yau, Kyle S., Hayashi, Yukiko K., Miyake, Noriko, Tsurusaki, Yoshinori, Doi, Hiroshi, Saitsu, HirotoVolume:
93
Langue:
english
Journal:
The American Journal of Human Genetics
DOI:
10.1016/j.ajhg.2013.05.004
Date:
July, 2013
Fichier:
PDF, 2.45 MB
english, 2013
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