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Article

A possible association of a human tektin-t gene mutation (A229V) with isolated non-syndromic asthenozoospermia: case report.

Human reproduction (Oxford, England) - 1 Apr 2008

Zuccarello Daniela, Ferlin Alberto, Garolla Andrea, Pati Mauro A, Moretti Afra, Cazzadore Carla, Francavilla Sandro, Foresta Carlo

Abstract excerpt

Asthenozoospermia (AZS), characterized by grade A + B sperm motility (as in World Health Organization Guidelines) < or =50% or A <25% in fresh ejaculate, may exist as an isolated disorder, in combination with other sperm anomalies or as part of syndromic association. The majority of syndromic patients can be ascribed to mutations in dynein genes, while, to date, no genes have been described to be associated in...

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PMID: 18227105
DOI: 10.1093/humrep/dem400

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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A possible association of a human tektin-t gene mutation (A229V) with isolated non-syndromic asthenozoospermia: case report.PMID 18227105Read ↗

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Absence of annulus in human asthenozoospermia: Case Report†Semantic proximity Read ↗

Aberrant Expression of Dynein light chain 1 (DYNLT1) is Associated with Human Male Factor Infertility*Semantic proximity Read ↗

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