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Article

FMR1 gene mutation screening by TP-PCR in patients with premature ovarian failure and fragile-X.

Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology - 1 Mar 2015

Tural Sengul, Tekcan Akın, Kara Nurten, Elbistan Mehmet, Güven Davut, Ali Tasdemir Haydar

Abstract excerpt

CGG repeat expansion in the FMR1 gene is associated with fragile X syndrome, fragile X-associated tremor/ ataxia syndrome and fragile X-associated primary ovarian insufficiency. In this study, FMR1 gene mutation screening was carried out in 50 patients. Among them, 12 (%24) were POF and 19 (%38)...

Read the complete abstract on PubMed

Topics

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Share to Alleles
Share to DNA Mutational Analysis
Share to Fragile X Mental Retardation Protein

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Fragile X Syndrome

Share to Menopause, Premature

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Share to Polymerase Chain Reaction

Share to Primary Ovarian Insufficiency

Source

Identifiers

PMID: 25366135
DOI: 10.3109/09513590.2014.975685

Genes

FMR1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-25366135-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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