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Heterozygous Variants in CTR9, Which Encodes a Major Component of the PAF1 Complex, Are Associated with a Neurodevelopmental Disorder.

Marije Meuwissen,Aline Verstraeten,Emmanuelle Ranza,Justyna Iwaszkiewicz,Maaike Bastiaansen,Ligia Mateiu,Merlijn Nemegeer,Josephina A. N. Meester,Alexandra Afenjar,Michelle Amaral,Diana Ballhausen,Sarah Barnett,Magalie Barth,Bob Asselbergh, Katrien Spaas,Bavo Heeman,Jennifer Bassetti,Patrick Blackburn,Marie Schaer,Xavier Blanc,Vincent Zoete,Kari Casas,Thomas Courtin,Diane Doummar,Frederic Guerry,Boris Keren,John Pappas,Rachel Rabin,Amber Begtrup,Marwan Shinawi,Anneke T. Vulto-van Silfhout,Tjitske Kleefstra,Matias Wagner,Alban Ziegler,Elise Schaefer,Benedicte Gerard,Charlotte De Bie,Sjoerd J. B. Holwerda,Mary Alice Abbot,Stylianos E. Antonarakis,Bart Loeys

Genetics in Medicine（2022）

Cited 3|Views46
Key words
Autism spectrum disorder,CTR9,Intellectual disability,Neurodevelopmental disorder,PAF1C
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