A homozygous mutation in RNU4ATAC as a cause of microcephalic osteodysplastic primordial dwarfism type I (MOPD I) with associated pigmentary disorder-Reference-Cited by-同舟云学术

A homozygous mutation in RNU4ATAC as a cause of microcephalic osteodysplastic primordial dwarfism type I (MOPD I) with associated pigmentary disorder

Published:2011-10-11 Issue:11 Volume:155 Page:2885-2896
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Abdel-Salam Ghada M.H.,Miyake Noriko,Eid Maha M.,Abdel-Hamid Mohamed S.,Hassan Nihal A.,Eid Ola M.,Effat Laila K.,El-Badry Tarek H.,El-Kamah Ghada Y.,El-Darouti Mohamed,Matsumoto Naomichi

Publisher

Wiley

Subject

Genetics(clinical),Genetics

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