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CJCP  2020, Vol. 22 Issue (7): 790-795    DOI: 10.7499/j.issn.1008-8830.1912041
RARE DISEASE RESEARCH Current Issue| Next Issue| Archive| Adv Search  | 
Variant analysis on steroid 5-reductase type 2 deficiency caused by a novel SRD5A2 mutation
CHU Guo-Ming1, LI Ping-Ping2, CHANG Wen-Jing1, HE Rong1, ZHAO Yan-Yan1
Department of Clinical Genetics, Shengjing Hospital of China Medical University, Shenyang 110004, China