MAB21L1 loss of function causes a syndromic neurodevelopmental disorder with distinctive <i>c</i>erebellar, <i>o</i>cular, cranio<i>f</i>acial and <i>g</i>enital features (COFG syndrome)
Abolfazl Rad(Sabzevar University of Medical Sciences), Miriam Schmidts(University Medical Center Freiburg), Kolsoum Saeidi(Kerman University of Medical Sciences), Kiely N. James(Children’s Institute), A. Gulhan Ercan‐Sencicek(Yale University), Hülya Kayserili(Istanbul University), Zeineb Bakey(Radboud University Nijmegen), Rose‐Mary Boustany(Duke Medical Center), Umut Altunoğlu(Istanbul University), Ahmet Okay Çağlayan(Dokuz Eylül University), Natalie Hauser(National Institutes of Health), Kaman Wu(Radboud University Nijmegen), Afsaneh Sahebzamani(Kerman University of Medical Sciences), Reza Maroofian(National Hospital for Neurology and Neurosurgery), Gözde Yeşil(Bezmiâlem Vakıf Üniversitesi), Peter Bauer(Centogene (Germany)), Joseph G. Gleeson(Howard Hughes Medical Institute), Maryam Najafi(Radboud University Nijmegen), Rebecca Miller(Inova Health System), Valentina Stanley(Children’s Institute), Murat Günel(Yale Cancer Center)
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