Walker-Warburg syndrome and tectocerebellar dysraphia: A novel association caused by a homozygous DAG1 mutation
- Zvi Leibovitz*
- , Hanna Mandel
- , Tzipora C. Falik-Zaccai
- , Shani Ben Harouch
- , David Savitzki
- , Karina Krajden-Haratz
- , Liat Gindes
- , Mordechai Tamarkin
- , Dorit Lev
- , William B. Dobyns
- , Tally Lerman-Sagie
*Corresponding author for this work
- Technion-Israel Institute of Technology
- Edith Wolfson Medical Center Israel
- Bar-Ilan University
- Seattle Children's Hospital
Research output: Contribution to journal › Article › peer-review
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