Inherited mutation of the luteinizing hormone/choriogonadotropin receptor (LHCGR) in empty follicle syndrome

OBJECTIVE: To test by genomic analysis whether empty follicle syndrome (EFS) in a family with two affected sisters has a genetic basis. DESIGN: Whole-exome sequencing in the context of clinical genetics. SETTING: University hospital. PATIENT(S): Two women (36 and 32 years old at the time of the stud...

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Main Authors: Yariz, Kemal O., Walsh, Tom, Uzak, Asli, Spiliopoulos, Michail, Duman, Duygu, Onalan, Gogsen, King, Mary-Claire, Tekin, Mustafa
Formato: Artigo
Idioma:Inglês
Publicado em: 2011
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3143235/
https://ncbi.nlm.nih.gov/pubmed/21683950
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.fertnstert.2011.05.057
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