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Article

A homozygous nonsense mutation of PLCZ1 cause male infertility with oocyte activation deficiency

7 Mar 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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PMID: 32146562
DOI: 10.1007/s10815-020-01719-4

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A homozygous nonsense mutation of PLCZ1 cause male infertility with oocyte activation deficiencyPMID 32146562Read ↗

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SPERM FACTORS AND EGG ACTIVATION: The phenotype of PLCZ1-deficient mice.Semantic proximity Read ↗

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A maternally inherited autosomal point mutation in human phospholipase C zeta (PLCζ) leads to male infertility.Semantic proximity Read ↗

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Novel mutations in PLCZ1 lead to early embryonic arrest as a male factorSemantic proximity Read ↗

SPERM FACTORS AND EGG ACTIVATION: The structure and function relationship of sperm PLCZ1Semantic proximity Read ↗

Homozygous mutation of PLCZ1 leads to defective human oocyte activation and infertility that is not rescued by the WW-binding protein PAWP.Semantic proximity Read ↗

The identification of novel mutations in PLCZ1 responsible for human fertilization failure and a therapeutic intervention by artificial oocyte activationSemantic proximity Read ↗

SPERM FACTORS AND EGG ACTIVATION: Fertilization failure after human ICSI and the clinical potential of PLCZ1Semantic proximity Read ↗

Novel PLCZ1 mutation caused polyspermy during in vitro fertilization.Semantic proximity Read ↗

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