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 biallelic loss-of-function variants in ZP1 identified in an infertile female with empty follicle syndrome

16 Jun 2020

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to Genetic Syndromes and Imprinting
Share to Ovarian function and disorders
Share to Reproductive Biology and Fertility

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 32556881
DOI: 10.1007/s10815-020-01855-x

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Novel biallelic loss-of-function variants in ZP1 identified in an infertile female with empty follicle syndromePMID 32556881Read ↗

Novel ZP1 pathogenic variants identified in an infertile patient and a successful live birth following ICSI treatment.Semantic proximity Read ↗

Novel mutations in ZP1: Expanding the mutational spectrum associated with empty follicle syndrome in infertile women.Semantic proximity Read ↗

A Novel Homozygous Nonsense Mutation in ZP1 Causes Female Infertility due to Empty Follicle Syndrome.Semantic proximity Read ↗

Novel variants in ZP1, ZP2 and ZP3 associated with empty follicle syndrome and abnormal zona pellucida.Semantic proximity Read ↗

A novel homozygous nonsense ZP1 variant causes human female infertility associated with empty follicle syndrome (EFS)Semantic proximity Read ↗

Compound heterozygous ZP1 mutations cause empty follicle syndrome in infertile sistersSemantic proximity Read ↗

A ZP1 gene mutation in a patient with empty follicle syndrome: A case report and literature review.Semantic proximity Read ↗

Novel mutations in ZP2 and ZP3 cause female infertility in three patients.Semantic proximity Read ↗

A recurrent ZP1 variant is responsible for oocyte maturation defect with degenerated oocytes in infertile femalesSemantic proximity Read ↗

Novel mutations in ZP1 and ZP2 cause primary infertility due to empty follicle syndrome and abnormal zona pellucida.Semantic proximity Read ↗

Compound heterozygous <i>ZP1</i> mutations cause empty follicle syndrome in infertile sistersSemantic proximity Read ↗

Identification of a heterozygous variant of ZP2 as a novel cause of empty follicle syndrome in humans and miceSemantic proximity Read ↗

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