Loss of the arginine methyltranserase PRMT7 causes syndromic intellectual disability with microcephaly and brachydactyly
Kernohan, Kristin D., McBride, Arran, Xi, Yanwei, Martin, Nicole, Schwartzentruber, Jeremy, Dyment, David A., Majewski, Jacek, Blaser, Susan, Boycott, Kym M., Chitayat, DavidLanguage:
english
Journal:
Clinical Genetics
DOI:
10.1111/cge.12884
Date:
October, 2016
File:
PDF, 1.24 MB
english, 2016