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A novel missense mutation, GGC(Arg454)→TGC(Cys), of CYP11B1 gene identified in a Chinese family with
[期刊论文] 作者：YE Zheng-qin,ZHANG Man-na,ZHAN,
来源：中华医学杂志（英文版） 年份：2010
Background Steroid 11β-hydroxylase deficiency (11β-OHD), an autosomal recessive inherited disease, accounts for 5%-8% of congenital adrenal hyperplasia.It was...
A novel missense mutation, GGC(Arg454)→TGC(Cys), of CYP11B1 gene identified in a Chinese family with
[期刊论文] 作者：YE Zheng-qin,ZHANG Man-na,ZHAN,
来源：中华医学杂志（英文版） 年份：2004
Background Steroid 11β-hydroxylase deficiency (11β-OHD), an autosomal recessive inherited disease, accounts for 5%-8% of congenital adrenal hyperplasia.It was...
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