|
Literature for DOID 11782: astigmatism
Xenbase Articles

(

Mono-allelic KCNB2 variants lead to a neurodevelopmental syndrome caused by altered channel inactivation.,
Bhat S,Rousseau J,Michaud C,Lourenço CM,Stoler JM,Louie RJ,Clarkson LK,Lichty A,Koboldt DC,Reshmi SC,Sisodiya SM,Hoytema van Konijnenburg EMM,Koop K,van Hasselt PM,Démurger F,Dubourg C,Sullivan BR,Hughes SS,Thiffault I,Tremblay ES,Accogli A,Srour M,Blunck R,Campeau PM,
Am J Hum Genet. March 4, 2024; 111(4):1537-6605.
![]() |