Further delineation of familial polycystic ovary syndrome (PCOS) via whole-exome sequencing: PCOS-related rare FBN3 and FN1 gene variants are identified.

Karakaya, Cengiz; Çil, Aylin Pelin; Bilguvar, Kaya; Çakir, Tunahan; Karalok, Mete Hakan; Karabacak, Recep Onur; Caglayan, Ahmet Okay

Karakaya, Cengiz; Çil, Aylin Pelin; Bilguvar, Kaya; Çakir, Tunahan; Karalok, Mete Hakan; Karabacak, Recep Onur; Caglayan, Ahmet Okay.

Afiliación

Karakaya C; Department of Medical Biochemistry, Gazi University School of Medicine, Ankara, Turkey.
Çil AP; Division of Reproductive Endocrinology and Infertility, Department of Obstetrics, Gynecology, and Reproductive Sciences, Yale School of Medicine, New Haven, Connecticut, USA.
Bilguvar K; American Hospital Women's Health and Assisted Reproductive Center Guzelbahce Sok, Istanbul, Turkey.
Çakir T; Department of Genetics, Yale Center for Genome Analysis, Yale School of Medicine, New Haven, Connecticut, USA.
Karalok MH; Departments of Neurosurgery, Neurobiology and Genetics, Yale School of Medicine, New Haven, Connecticut, USA.
Karabacak RO; Department of Medical Genetics, Acibadem University School of Medicine, Istanbul, Turkey.
Caglayan AO; Department of Bioengineering, Gebze Technical University, Gebze, Turkey.

J Obstet Gynaecol Res ; 48(5): 1202-1211, 2022 May.

Article en En | MEDLINE | ID: mdl-35141985

Asunto(s)

Fibrilinas; Fibronectinas; Síndrome del Ovario Poliquístico; Femenino; Fibrilinas/genética; Fibronectinas/genética; Humanos; Síndrome del Ovario Poliquístico/genética; Secuenciación del Exoma

Palabras clave

PCOS; extracellular matrix; genetics; whole-exome sequencing

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Síndrome del Ovario Poliquístico / Fibronectinas / Fibrilinas Tipo de estudio: Prognostic_studies Límite: Female / Humans Idioma: En Revista: J Obstet Gynaecol Res Asunto de la revista: GINECOLOGIA / OBSTETRICIA Año: 2022 Tipo del documento: Article País de afiliación: Turquía Pais de publicación: Australia

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