Novel NR5A1 Missense Mutation in Premature Ovarian Failure: Detection in Han Chinese Indicates Causation in Different Ethnic Groups

BACKGROUND: The etiology of most premature ovarian failure (POF) cases is usually elusive. Although genetic causes clearly exist and a likely susceptible region of 8q22.3 has been discovered, no predominant explanation exists for POF. More recently, evidences have indicated that mutations in NR5A1 g...

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Detalles Bibliográficos
Autores principales: Jiao, Xue, Qin, Yingying, Li, Guangyu, Zhao, Shidou, You, Li, Ma, Jinlong, Simpson, Joe Leigh, Chen, Zi-Jiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3779243/
https://www.ncbi.nlm.nih.gov/pubmed/24073220
http://dx.doi.org/10.1371/journal.pone.0074759

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3779243/
https://www.ncbi.nlm.nih.gov/pubmed/24073220
http://dx.doi.org/10.1371/journal.pone.0074759

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