A non-senseMCM9mutation in a familial case of primary ovarian insufficiency-Reference-Cited by-同舟云学术

A non-senseMCM9mutation in a familial case of primary ovarian insufficiency

Author:

Fauchereau F.¹²,Shalev S.³⁴,Chervinsky E.³⁴,Beck-Fruchter R.⁵,Legois B.¹²,Fellous M.⁶⁷,Caburet S.¹²,Veitia R.A.¹²

Affiliation:

1. Institut Jacques Monod; Paris France

2. Department of Biology; Université Paris Diderot-Paris VII; Paris Cedex France

3. Department of Obstetrics and Gynecology; The Rappaport Faculty of Medicine; Haifa Israel

4. Genetic Institute; Haemek Medical Center; Afula Israel

5. OBGYN Department; Emek Medical Center; Afula Israel

6. Department of Genetics and Development; Institut Cochin; Paris France

7. Faculty of Medicine; Université Paris Descartes-Paris V; Paris France

Funder

Université Paris Diderot

Fondation pour la Recherche Médicale

Fondation Maladies Rares

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference12 articles.

1. Premature ovarian failure;Beck-Peccoz;Orphanet J Rare Dis,2006

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