Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Novel compound heterozygous variants of DNAH17 in a Chinese infertile man with multiple morphological abnormalities of sperm flagella.

Andrologia - 1 Nov 2022

Liu Zhonglin, Wang Chunyan, Ni Feng, Yang Fenglian, Wei Han, Li Tengyan, Wang Junli, Wang Binbin

Abstract excerpt

Multiple morphological abnormalities of the sperm flagellum (MMAF) have been reported to be an important cause of male infertility and reflect a heterogeneous genetic disorder. Previous studies have identified dozens of candidate pathogenic genes for MMAF, but the aetiology in approximately 50% of cases remains unexplained. The present study aimed to identify novel potentially pathogenic gene variants of MMAF. A...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Amino Acids
Share to Axonemal Dyneins

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Infertility, Male

Share to Mutation

Share to Sperm Tail

Share to Spermatozoa

Source

Identifiers

PMID: 35932098
DOI: 10.1111/and.14553

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Novel compound heterozygous variants of DNAH17 in a Chinese infertile man with multiple morphological abnormalities of sperm flagella.PMID 35932098Read ↗

Bi-allelic DNAH8 Variants Lead to Multiple Morphological Abnormalities of the Sperm Flagella and Primary Male Infertility.Semantic proximity Read ↗

DNAH17 is associated with asthenozoospermia and multiple morphological abnormalities of sperm flagella.Semantic proximity Read ↗

Mutations in DNAH8 contribute to multiple morphological abnormalities of sperm flagella and male infertility.Semantic proximity Read ↗

Novel mutations in DNAH17 cause sperm flagellum defects and their influence on ICSI outcome.Semantic proximity Read ↗

Novel compound heterozygous mutations in DNAH1 cause primary infertility in Han Chinese males with multiple morphological abnormalities of the sperm flagella.Semantic proximity Read ↗

Identification of Novel Mutation Sites in DNAH1 of Multiple Morphological Anomalies of the Flagella PatientsSemantic proximity Read ↗

Novel loss-of-function variants in DNAH17 cause multiple morphological abnormalities of the sperm flagella in humans and mice.Semantic proximity Read ↗

Novel bi-allelic variants in DNAH10 lead to multiple morphological abnormalities of sperm flagella and male infertility.Semantic proximity Read ↗

A DNAH17 missense variant causes flagella destabilization and asthenozoospermia.Semantic proximity Read ↗

Bi-allelic variants in DNAH10 cause asthenoteratozoospermia and male infertility.Semantic proximity Read ↗

Identification of DNAH6 mutations in infertile men with multiple morphological abnormalities of the sperm flagellaSemantic proximity Read ↗

A novel NPHP4 homozygous missense variant identified in infertile brothers with multiple morphological abnormalities of the sperm flagella.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.