STX2 is a causative gene for nonobstructive azoospermia
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DOI: 10.1002/humu.23423
Abstract: STX2 encodes a sulfoglycolipid transporter. Although Stx2 nullizygosity is known to cause spermatogenic failure in mice, STX2 mutations have not been identified in humans. Here, we performed STX2 mutation analysis for 131 Japanese men clinically… read more here.
Keywords: nonobstructive azoospermia; stx2 causative; stx2; mutation ... See more keywords