Homozygous variants in SYCP2L cause premature ovarian insufficiency

BACKGROUND: The genetic causes of the majority of cases of female infertility caused by premature ovarian insufficiency (POI) are unknown. OBJECTIVE: To identify the genetic causes of POI in 110 patients. METHODS: Whole-exome sequencing was performed on 110 patients with POI, and putative disease-ca...

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Detalles Bibliográficos
Autores principales: He, Wen-Bin, Tan, Chen, Zhang, Ya-Xin, Meng, Lan-Lan, Gong, Fei, Lu, Guang-Xiu, Lin, Ge, Du, Juan, Tan, Yue-Qiu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2021
Materias:
Novel Disease Loci
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7907585/
https://www.ncbi.nlm.nih.gov/pubmed/32303603
http://dx.doi.org/10.1136/jmedgenet-2019-106789

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7907585/
https://www.ncbi.nlm.nih.gov/pubmed/32303603
http://dx.doi.org/10.1136/jmedgenet-2019-106789

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