Chowdhury, Fuad
Wang, Lei
Al-Raqad, Mohammed
Amor, David J.
Baxová, Alice
Bendová, Šárka
Biamino, Elisa
Brusco, Alfredo
Caluseriu, Oana
Cox, Nancy J.
Froukh, Tawfiq
Gunay-Aygun, Meral
Hančárová, Miroslava
Haynes, Devon
Heide, Solveig
Hoganson, George
Kaname, Tadashi
Keren, Boris
Kosaki, Kenjiro
Kubota, Kazuo
Lemons, Jennifer M.
Magriña, Maria A.
Mark, Paul R.
McDonald, Marie T.
Montgomery, Sarah
Morley, Gina M.
Ohnishi, Hidenori
Okamoto, Nobuhiko
Rodriguez-Buritica, David
Rump, Patrick
Sedláček, Zdeněk
Schatz, Krista
Streff, Haley
Uehara, Tomoko
Walia, Jagdeep S.
Wheeler, Patricia G.
Wiesener, Antje
Zweier, Christiane
Kawakami, Koichi
Wentzensen, Ingrid M.
Lalani, Seema R.
Siu, Victoria M.
Bi, Weimin
Balci, Tugce B. http://orcid.org/0000-0002-5409-8387
Funding for this research was provided by:
Schulich School of Medicine and Dentistry (SROP, SROP, SROP)
Ministero dell’Istruzione, dell’Università e della Ricerca (D15D18000410001)
National Institute of Mental Health (MH111661)
Japan Agency for Medical Research and Development (16ek0109166h0002, 17ek0109151s1)
Japan Society for the Promotion of Science (JP18K07863)
This article is maintained by: Elsevier
Article Title: Haploinsufficiency of PRR12 causes a spectrum of neurodevelopmental, eye, and multisystem abnormalities
Journal Title: Genetics in Medicine
CrossRef DOI link to publisher maintained version: https://doi.org/10.1038/s41436-021-01129-6
Content Type: article
Copyright: © 2021, The Author(s), under exclusive licence to the American College of Medical Genetics and Genomics