Biallelic variants in INTS11 are associated with a novel complex neurological disorder
Marcello Niceta,Tepe Burak, Erica Macke, Monika Hubshman,Oguz Kanca,Laura Schultz-Rogers,Yuri Zarate, Bradley Schaefer,Jorge Luis Granadillo De Luque,Daniel Wegner,Benjamin Cogne,Brigitte Gilbert-Dussardier,Xavier Le Guillou,Eric Wagner, Lynn Pais, Jennifer Neil, Ganeshwaran Mochida, Chris Walsh,Nurit Magal,Valerie Drasinover,Mordechai Shohat,Tanya L. Schwab,Christopher Schmitz,Karl J. Clark, Anthony Fine, Brendan C. Lanpher, Ralitza Gavrilova, Pierre Blanc,Lydie Burglen,Alexandra Afenjar,Dora Steel,Manju Kurian, Prab Prabhaker, Sophie Goesswein,Nataliya Di Donato, Enrico Bertini,Michael Wangler,Shinya Yamamoto,Marco Tartaglia, Eric W. Klee,Hugo J. Bellen EUROPEAN JOURNAL OF HUMAN GENETICS(2024)
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