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Homozygous loss of DIAPH1 is a novel cause of microcephaly in humans
Ercan-Sencicek, A Gulhan, Jambi, Samira, Franjic, Daniel, Nishimura, Sayoko, Li, Mingfeng, El-Fishawy, Paul, Morgan, Thomas M, Sanders, Stephan J, Bilguvar, Kaya, Suri, Mohnish, Johnson, Michele H, GuVolume:
23
Language:
english
Journal:
European Journal of Human Genetics
DOI:
10.1038/ejhg.2014.82
Date:
February, 2015
File:
PDF, 1.53 MB
english, 2015