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Article

Novel mutations in PMFBP1 , TSGA10 and SUN5 : Expanding the spectrum of mutations that may cause acephalic spermatozoa

13 Apr 2020

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Share to Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
Share to Reproductive Biology and Fertility
Share to Sperm and Testicular Function

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 32285443
DOI: 10.1111/cge.13747

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Related research

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Novel mutations in PMFBP1 , TSGA10 and SUN5 : Expanding the spectrum of mutations that may cause acephalic spermatozoaPMID 32285443Read ↗

[Advances in the molecular genetic studies of acephalic spermatozoa syndrome].Semantic proximity Read ↗

Novel Mutation and Deletion in SUN5 Cause Male Infertility with Acephalic Spermatozoa SyndromeSemantic proximity Read ↗

Loss-of-function mutation in TSGA10 causes acephalic spermatozoa phenotype in human.Semantic proximity Read ↗

Biallelic SUN5 Mutations Cause Autosomal-Recessive Acephalic Spermatozoa SyndromeSemantic proximity Read ↗

A novel homozygous missense mutation of PMFBP1 causes acephalic spermatozoa syndrome.Semantic proximity Read ↗

Mutations in PMFBP1 Cause Acephalic Spermatozoa Syndrome.Semantic proximity Read ↗

Patients with acephalic spermatozoa syndrome linked to novel TSGA10/PMFBP1 variants have favorable pregnancy outcomes from intracytoplasmic sperm injection.Semantic proximity Read ↗

Genetic contribution of SUN5 mutations to acephalic spermatozoa in Fujian China.Semantic proximity Read ↗

[Clinical characteristics and genetic analysis of a patient with Acephalic spermatozoa syndrome due to variant of PMFBP1 gene].Semantic proximity Read ↗

Pathogenesis of acephalic spermatozoa syndrome caused by PMFBP1 mutationSemantic proximity Read ↗

Pathogenesis of acephalic spermatozoa syndrome caused by splicing mutation and de novo deletion in TSGA10.Semantic proximity Read ↗

<i>TSGA10</i> is a novel candidate gene associated with acephalic spermatozoaSemantic proximity Read ↗

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