Cite
HARVARD Citation
Perez, Y. et al. (2017). A Rare Variant in PGAP2 Causes Autosomal Recessive Hyperphosphatasia with Mental Retardation Syndrome, with a Mild Phenotype in Heterozygous Carriers. BioMed research international. p. . [Online].
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Perez, Y. et al. (2017). A Rare Variant in PGAP2 Causes Autosomal Recessive Hyperphosphatasia with Mental Retardation Syndrome, with a Mild Phenotype in Heterozygous Carriers. BioMed research international. p. . [Online].