Two mutations in the axonemal dynein heavy chain gene 5 in a Chinese asthenozoospermia patient-Reference-Cited by-同舟云学术

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Two mutations in the axonemal dynein heavy chain gene 5 in a Chinese asthenozoospermia patient

Published:2020-07-10 Issue:28 Volume:99 Page:e20813
ISSN:0025-7974
Container-title:Medicine
language:en
Short-container-title:

Author:

He Jing,Li Leilei,Yu Yang,Hu Xiaonan,Zhang Hongguo,Liu Ruizhi,Wang Ruixue

Funder

Clinical Medical Research Special Funds of Chinese Medical Association, P.R. China

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

General Medicine

Reference12 articles.

1. Asthenozoospermia: analysis of a large population;Curi;Arch Androl,2009

2. Mutations in DNAH5 cause primary ciliary dyskinesia and randomization of left-right asymmetry;Olbrich;Nat Genet,2002

3. Primary ciliary dyskinesia: clinical presentation, diagnosis and genetics;Storm van's Gravesande;Ann Med,2005

4. Genetic defects in ciliary structure and function;Zariwala;Annu Rev Physiol,2007

5. Mutations in dynein genes in patients affected by isolated non-syndromic asthenozoospermia;Zuccarello;Hum Reprod,2008

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2. Research progress on ion channels and their molecular regulatory mechanisms in the human sperm flagellum;The FASEB Journal;2023-06-23

3. Homozygous mutation in DNALI1 leads to asthenoteratozoospermia by affecting the inner dynein arms;Frontiers in Endocrinology;2023-01-16

4. Potential role of dynein‐related genes in the etiology of male infertility: A systematic review and a meta‐analysis;Andrology;2022-09-11

5. Novel compound heterozygous variants of DNAH17 in a Chinese infertile man with multiple morphological abnormalities of sperm flagella;Andrologia;2022-08-05

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