학술논문
Rare PHEX intron variant causes complete and severe phenotype in a family with hypophosphatemic rickets: A case report
Document Type
Article
Author
Source
In: Journal of Pediatric Endocrinology and Metabolism . (Journal of Pediatric Endocrinology and Metabolism, 1 January 2023, 36(1):91-95)
Subject
Language
English
ISSN
21910251
0334018X
0334018X