Intronic variation of the SOHLH2 gene confers risk to male reproductive impairment

Volume: 114, Issue: 2, Pages: 398 - 406
Published: Aug 1, 2020
Abstract
Objective null To evaluate whether SOHLH2 intronic variation contributes to the genetic predisposition to male infertility traits, including severe oligospermia (SO) and different nonobstructive azoospermia (NOA) clinical phenotypes. null null null Design null Genetic association study. null null null Setting null Not applicable. null null null Patient(s) null Five hundred five cases (455 infertile patients diagnosed with NOA and 50 with SO) and...
Paper Details
Title
Intronic variation of the SOHLH2 gene confers risk to male reproductive impairment
Published Date
Aug 1, 2020
Volume
114
Issue
2
Pages
398 - 406
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