| Literature DB >> 33646398 |
Judith Sebestyen VanSickle1, Tarak Srivastava2, Penny Monachino2, Uri S Alon2.
Abstract
Entities:
Keywords: ADHR; Autosomal dominant hypophosphatemic rickets; Child; FGF23 mutation; Hypophosphatemic rickets; Iron deficiency
Year: 2021 PMID: 33646398 DOI: 10.1007/s00467-021-05012-z
Source DB: PubMed Journal: Pediatr Nephrol ISSN: 0931-041X Impact factor: 3.714