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Analysis of CYP21A2 gene mutation and phenotype in patients with 21-hydroxylase deficiency
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作者 舒剑波 《China Medical Abstracts(Internal Medicine)》 2019年第2期83-83,共1页
Objective To investigate the spectrum of CYP21A2gene mutation and the correlation between genotype and phenotype in patients with 21-hydroxylase deficiency in Tianjin and surrounding areas. Methods Genomic DNA was ext... Objective To investigate the spectrum of CYP21A2gene mutation and the correlation between genotype and phenotype in patients with 21-hydroxylase deficiency in Tianjin and surrounding areas. Methods Genomic DNA was extracted from the peripheral blood samples of the proband. 展开更多
关键词 CYP ANALYSIS of CYP21A2 GENE MUTATION 21-hydroxylase deficiency
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