We found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleNext generation sequencing in a family with autosomal recessive Kahrizi syndrome (OMIM 612713) reveals a homozygous frameshift mutation in SRD5A3.AuthorsKahrizi, Kimia; Hu, Cougar Hao; Garshasbi, Masoud; Abedini, Seyedeh Sedigheh; Ghadami, Shirin; Kariminejad, Roxana; Ullmann, Reinhard; Chen, Wei; Ropers, H-Hilger; Kuss, Andreas W; Najmabadi, Hossein; Tzschach, AndreasPublicationEuropean Journal of Human Genetics, 2011, Vol 19, Issue 1, p115ISSN1018-4813Publication typearticleDOI10.1038/ejhg.2010.132