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: Medical Molecular Genetics Department, Human Genetics and Genome Research Division
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