A complex heterozygous mutation of His373Leu and Asp487–Ser488–Phe489 deletion in human cytochrome P450c17 causes 17α-hydroxylase/17,20-lyase deficiency in three Chinese sisters

✍ Scribed by Jie Qiao; Ren-Ming Hu; Yong-De Peng; Huai-Dong Song; Yi-Wen Peng; Guo-Feng Gao; Jian-Hua Hao; Nan-Ying Hu; Man-Yin Xu; Jia-Lun Chen

• Book ID: 117463117
• Publisher: Elsevier Science
• Year: 2003
• Tongue: English
• Weight: 377 KB
• Volume: 201
• Category: Article
• ISSN: 0303-7207
• DOI: 10.1016/s0303-7207(02)00156-9