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Article

A novel PPRC1 point mutation in a Chinese family with premature ovarian failure: A case study.

The journal of gene medicine - 1 Jun 2021

Zhang Xiao-Jin, Gu Yu, Fu Wei

Abstract excerpt

BACKGROUND: Patients with premature ovarian failure (POF) have an at least 6-month history of amenorrhea and elevated follicle-stimulating hormone levels in plasma. Most of the POF causes are idiopathic and hereditary, and chromosomal abnormalities have been associated with POF development. A pedigree study was performed on a family with idiopathic POF to observe the possible link between gene mutation and POF...

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PMID: 33818872
DOI: 10.1002/jgm.3335

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