Identification of potential causal variants for premature ovarian failure by whole exome sequencing
Abstract Background Premature ovarian failure (POF) is a highly heterogeneous disorder that occurs in 1% of women of reproductive age. Very few causative genes and variants contributing to POF have been detected, and the disease remains incompletely understood. In this study, we used whole exome seq...
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Main Authors: | , , , , , , , |
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Format: | Book |
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BMC,
2020-10-01T00:00:00Z.
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A1234.567 |
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