Exome sequencing reveals SYCE1 mutation associated with autosomal recessive primary ovarian insufficiency

Liat De Vries*, Doron M. Behar, Pola Smirin-Yosef, Irina Lagovsky, Shay Tzur, Lina Basel-Vanagaite

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

126 Scopus citations

Fingerprint

Dive into the research topics of 'Exome sequencing reveals SYCE1 mutation associated with autosomal recessive primary ovarian insufficiency'. Together they form a unique fingerprint.

Medicine & Life Sciences

Chemistry