Perez, Y., Wormser, O., Sadaka, Y., Birk, R., Narkis, G., & Birk, O. S. (2017). A Rare Variant in PGAP2 Causes Autosomal Recessive Hyperphosphatasia with Mental Retardation Syndrome, with a Mild Phenotype in Heterozygous Carriers. Biomed Res Int.
Chicago Style citaatPerez, Yonatan, Ohad Wormser, Yair Sadaka, Ruth Birk, Ginat Narkis, en Ohad S. Birk. "A Rare Variant in PGAP2 Causes Autosomal Recessive Hyperphosphatasia With Mental Retardation Syndrome, With a Mild Phenotype in Heterozygous Carriers." Biomed Res Int 2017.
MLA citatiePerez, Yonatan, et al. "A Rare Variant in PGAP2 Causes Autosomal Recessive Hyperphosphatasia With Mental Retardation Syndrome, With a Mild Phenotype in Heterozygous Carriers." Biomed Res Int 2017.
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