Rare variant enrichment analysis supports GREB1L as a contributory driver gene in the etiology of Mayer-Rokitansky-Küster-Hauser syndrome
Titel:
Rare variant enrichment analysis supports GREB1L as a contributory driver gene in the etiology of Mayer-Rokitansky-Küster-Hauser syndrome
Auteur:
Jolly, Angad Du, Haowei Borel, Christelle Chen, Na Zhao, Sen Grochowski, Christopher M. Duan, Ruizhi Fatih, Jawid M. Dawood, Moez Salvi, Sejal Jhangiani, Shalini N. Muzny, Donna M. Koch, André Rouskas, Konstantinos Glentis, Stavros Deligeoroglou, Efthymios Bacopoulou, Flora Wise, Carol A. Dietrich, Jennifer E. Van den Veyver, Ignatia B. Dimas, Antigone S. Brucker, Sara Sutton, V. Reid Gibbs, Richard A. Antonarakis, Stylianos E. Wu, Nan Coban-Akdemir, Zeynep H. Zhu, Lan Posey, Jennifer E. Lupski, James R.