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Consanguineous familial study revealed biallelic FIGLA mutation associated with premature ovarian insufficiency

Abstract Background To dissect the genetic alteration in two sisters with premature ovarian insufficiency (POI) from a consanguineous family. Methods Whole-exome sequencing technology was used in the POI proband, bioinformatics analysis was carried out to identify the potential genetic cause in this...

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Main Authors: Beili Chen (Author), Lin Li (Author), Jing Wang (Author), Tengyan Li (Author), Hong Pan (Author), Beihong Liu (Author), Yiran Zhou (Author), Yunxia Cao (Author), Binbin Wang (Author)
Format: Book
Published: BMC, 2018-06-01T00:00:00Z.
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