ArticleJournal of human genetics2016
A de novo mosaic mutation of PHEX in a boy with hypophosphatemic rickets.
Chen Weng et al.PubMed ↗Publisher ↗
No numbers read from the abstract.
10 papers cite it
this papercites it
ArticleJournal of human genetics2016
Chen Weng et al.PubMed ↗Publisher ↗
No numbers read from the abstract.