Severe neurological manifestations in an Egyptian patient with a novel frameshift mutation in the Glutaryl-CoA dehydrogenase gene
暂无分享,去创建一个
R. El Bekay | H. Zayed | A. Ouhtit | S. Mohammad | O. Zaki | H. E. El Abd | U. Abdel-Motal | Magdy M. Hassan | Ahmed Moseilhy