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: | , , , , , , , , |
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Format: | Book |
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BMC,
2018-06-01T00:00:00Z.
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