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Analysis of CYP21A2 gene mutation and phenotype in patients with 21-hydroxylase deficiency

作者:舒剑波cypanalysisofcyp21a2genemutationdeficiency

摘要: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.

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中国医学文摘·耳鼻咽喉科学

《中国医学文摘·耳鼻咽喉科学》是一本有较高学术价值的双月刊,自创刊以来,选题新奇而不失报道广度,服务大众而不失理论高度,颇受业界和广大读者的关注和好评。

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