Compound heterozygous KCTD19 variants in a man with isolated nonobstructive azoospermia

Compound heterozygous KCTD19 variants in a man with isolated nonobstructive azoospermia

Abstract Case A 40‐year‐old Japanese man with nonobstructive azoospermia (NOA) was found to carry rare variants in KCTD19, a newly identified causative gene for spermatogenic failure. This patient was identified through mutation screening of KCTD19 in 97 men with etiology‐unknown isolated NOA. Outco...

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Main Authors: Yuki Muranishi, Yuko Katoh‐Fukui, Atsushi Hattori, Yoshitomo Kobori, Akiyoshi Osaka, Hiroshi Okada, Toshiyuki Iwahata, Masafumi Kon, Nobuo Shinohara, Maki Fukami
Format: Article
Language:English
Published: Wiley 2024-01-01
Series:Reproductive Medicine and Biology
Subjects:
azoospermia
compound heterozygosity
long‐read sequencing
maturation arrest
mutation
Online Access:https://doi.org/10.1002/rmb2.12608
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https://doi.org/10.1002/rmb2.12608

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