Novel STAG3 mutations in a Caucasian family with primary ovarian insufficiency
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics,Molecular Biology,General Medicine
Link
http://link.springer.com/content/pdf/10.1007/s00438-019-01594-4.pdf
Reference31 articles.
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3. Carramolino L, Lee BC, Zaballos A, Peled A, Barthelemy I, Shav-Tal Y, Prieto I, Carmi P, Gothelf Y, González de Buitrago G, Aracil M, Márquez G, Barbero JL, Zipori D (1997) SA-1, a nuclear protein encoded by one member of a novel gene family: molecular cloning and detection in hemopoietic organs. Gene 195:151–159
4. Colombo R, Pontoglio A, Bini M (2017) A STAG3 missense mutation in two sisters with primary ovarian insufficiency. Eur J Obstet Gynecol Reprod Biol 216:269–271
5. Fouquet B, Pawlikowska P, Caburet S, Guigon C, Mäkinen M, Tanner L, Hietala M, Urbanska K, Bellutti L, Legois B, Bessieres B, Gougeon A, Benachi A, Livera G, Rosselli F, Veitia RA, Misrahi M (2017) A homozygous FANCM mutation underlies a familial case of non-syndromic primary ovarian insufficiency. Elife. https://doi.org/10.7554/elife.30490
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