IVS9-9C>A, not IVS9-9A>C, mutation in CYP21A2 causes classic salt-wasting steroid 21-hydroxylase deficiency

Saved in:
Bibliographic Details
Published in:Metabolism, clinical and experimental clinical and experimental, 2010, Vol.59 (10), p.e12-e12
Main Authors: Katsumata, Noriyuki, Shinagawa, Takashi, Horikawa, Reiko, Fujikura, Kaori
Format: Article
Language:English
Subjects:
Endocrinology & Metabolism
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:
ISSN:0026-0495
1532-8600
DOI:10.1016/j.metabol.2010.06.011