<i>WT1</i>, <i>NR0B1</i>, <i>NR5A1</i>, <i>LHX9</i>, <i>ZFP92</i>, <i>ZNF275</i>, <i>INSL3</i>, and <i>NRIP1</i> Genetic Variants in Patients with Premature Ovarian Insufficiency in a Mexican Cohort
Premature ovarian insufficiency (POI) is one of the main causes of female premature infertility. POI is a genetically heterogeneous disorder with a complex molecular etiology; as such, the genetic causes remain unknown in the majority of patients. Therefore, this study aimed to identify mutations an...
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| Format: | Article |
| Language: | English |
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MDPI AG
2022-03-01
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| Series: | Genes |
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| Online Access: | https://www.mdpi.com/2073-4425/13/4/611 |