학술논문
Excluding Digenic Inheritance of PGAP2 and PGAP3 Variants in Mabry Syndrome (OMIM 239300) Patient: Phenotypic Spectrum Associated with PGAP2 Gene Variants in Hyperphosphatasia with Mental Retardation Syndrome-3 (HPMRS3)
Document Type
Article
Author
Source
In: Genes . (Genes, February 2023, 14(2))
Subject
Language
English
ISSN
20734425