A human de novo mutation in MYH10...

Rare Diseases 2013 / 01 Vol. 1; Iss. 1

A human de novo mutation in MYH10 phenocopies the loss of function mutation in mice

Tuzovic, Lea, Yu, Lan, Zeng, Wenqi, Li, Xiang, Lu, Hong, Lu, Hsiao-Mei, Gonzalez, Kelly DF, Chung, Wendy K
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Volume:
1
Language:
english
Journal:
Rare Diseases
DOI:
10.4161/rdis.26144
Date:
January, 2013
File:
PDF, 324 KB
english, 2013
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