https://www.selleckchem.com/
B*40450 differs from B*40010201 by one nucleotide substitution at position 5 in exon 1. This article is protected by copyright. All rights reserved. Congenital bilateral absence of vas deferens (CBAVD) is an important disease of male infertility, which affects 1%-2% of infertile population. In addition to common mutations of CFTR, copy number variants (CNVs) have also been implicated as one of the pathogenesis of CBAVD. The present study aimed to investigate the genetic contribution of CFTR CNVs in Chinese Han population with CBAVD. Two hundred and sixty-th
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