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

Journal article

Peer reviewed

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

Clinical genetics, Vol.89(5), pp.608-613

05/2016

PMID: 26848058

Abstract

BMP15

GDF9

NOBOX

primary ovarian insufficiency

1 Record Views

Title: NOBOX is a strong autosomal candidate gene in Tunisian patients with primary ovarian insufficiency
Creators - without role: N. Bouali - Hôpital Farhat Hached
B. Francou - Inserm
J. Bouligand - Inserm
B. Lakhal - Hôpital Farhat Hached
I. Malek - Hôpital Farhat Hached
M. Kammoun - Hôpital Farhat Hached
J. Warszawski - Bicêtre Hospital
S. Mougou - Hôpital Farhat Hached
A. Saad - Hôpital Farhat Hached
A. Guiochon-Mantel - Inserm
Publication Details: Clinical genetics, Vol.89(5), pp.608-613
Publisher: Blackwell Publishing Ltd
Number of pages: 6
Identifiers: 9931875608331
Academic Unit: University Ha'il
Language: English
Resource Type: Journal article