Exome Sequencing Identifies INPPL1 Mutations as a Cause of Opsismodysplasia
Huber, Céline, Faqeih, Eissa Ali, Bartholdi, Deborah, Bole-Feysot, Christine, Borochowitz, Zvi, Cavalcanti, Denise P., Frigo, Amandine, Nitschke, Patrick, Roume, Joelle, Santos, Heloísa G., Shalev, StVolume:
92
Language:
english
Journal:
The American Journal of Human Genetics
DOI:
10.1016/j.ajhg.2012.11.015
Date:
January, 2013
File:
PDF, 310 KB
english, 2013