Work

NOBOX is a strong autosomal candidate gene in Tunisian patients with primary ovarian insufficiency

Year: 2016

Type: article

Study design: Observational Study

Source: Clinical Genetics

DOI: 10.1111/cge.12750

Authors: N. Bouali, B. Francou, J. Bouligand, B. Lakhal, I. Malek, M. Kammoun, J. Warszawski, S. Mougou, A. Saad, A. Guiochon‐Mantel

Institutions: Hôpital Farhat Hached, Inserm, Université Paris-Saclay, Assistance Publique – Hôpitaux de Paris, Bicêtre Hospital, Université Paris-Sud

Language: English

Topic: Ovarian function and disorders

Subfield: Reproductive Medicine

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: closed

Funders: Ministère de l'Enseignement Supérieur et de la Recherche Scientifique, Assistance Publique - Hôpitaux de Paris

OpenAlex ID: W2294528688

FWCI: 3.89

Cites: 20

Cited by: 24

Related to: 10