DOI: 10.1111/cge.13033 , , PMID: 28390064 Issn Print: 0009-9163 Publication Date: 2018/01/01 Print Facebook Twitter LinkedIn Email PGAP3‐related hyperphosphatasia with mental retardation syndrome: Report of 10 new patients and a homozygous founder mutation M.S. Abdel‐Hamid; M.Y. Issa; G.A. Otaify; S.F. Abdel‐Ghafar; H.M. Elbendary; M.S. Zaki + Author Information Author Information: Medical Molecular Genetics Department, Human Genetics and Genome Research Division Checking for direct PDF access through Ovid View on Journal Site Abstract Abstract unavailable for this article.