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A homozygous truncating variant in GDF9 in siblings with primary ovarian insufficiency
Premature or primary ovarian insufficiency (POI) affects approximately 1% of women and can be due to a variety of causes. Genetic causes include syndromic and non-syndromic POI. There are several promising candidate genes for whom a clear Mendelian association with non-syndromic POI has not yet been...
में बचाया:
| में प्रकाशित: | J Assist Reprod Genet |
|---|---|
| मुख्य लेखकों: | , , , , , |
| स्वरूप: | Artigo |
| भाषा: | Inglês |
| प्रकाशित: |
Springer US
2021
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| विषय: | |
| ऑनलाइन पहुंच: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8266936/ https://ncbi.nlm.nih.gov/pubmed/33797006 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10815-021-02144-x |
| टैग : |
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