Identification of novel and rare CYP21A2 variants in Chinese patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

Xu, Jing

Identification of novel and rare CYP21A2 variants in Chinese patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency. [electronic resource] - Clinical biochemistry Jun 2019 - 44-49 p. digital

Publication Type: Journal Article

1873-2933

10.1016/j.clinbiochem.2019.04.008 doi


Adrenal Hyperplasia, Congenital--genetics
Asian People--genetics
Humans
Mutation
Pseudogenes--genetics
Retrospective Studies