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Literature for DOID 9834: hyperopia
Xenbase Articles

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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.
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