A novel Compound Heterozygous Mutations causing 21-Hydroxylase Deficiency

Home
About Journal
Editorial Board
Current Issue
Archive
Subscription
Open Access
Contact Us
中文

A novel Compound Heterozygous Mutations causing 21-Hydroxylase Deficiency Basic & Clinical Medicine . 2012, (6): 660 -663 .

京ICP备07012236号
Website Copyright © Basic & Clinical Medicine

Add: 5 Dong Dan San Tiao, Beijing 100005
Tel: 010-69156964； 010-65273665
E-mail: basic_clinic@vip.163.com
Website: http://jcyxylc.pumc.edu.cn