hyperopia

Literature (2)

Literature for DOID 9834: hyperopia

Xenbase Articles Publications associated with this Disease Ontology entry or its descendants

:
(

Denotes literature images)

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.
A shared mechanism in eye optical development: Lens nucleus centralization in Xenopuslaevis., Garcia KA,Tseng KA,Vorontsova I, Exp Eye Res. March 17, 2026; 267:0014-4835.

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.

A shared mechanism in eye optical development: Lens nucleus centralization in Xenopuslaevis., Garcia KA,Tseng KA,Vorontsova I, Exp Eye Res. March 17, 2026; 267:0014-4835.