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Summary Literature (3)
Literature for DOID 0050564: autosomal dominant nonsyndromic deafness

Xenbase Articles :
( Denotes literature images)
Altered gating properties of functional Cx26 mutants associated with recessive non-syndromic hearing loss., Meşe G,Londin E,Mui R,Brink PR,White TW, Hum Genet. August 1, 2004; 115(3):1432-1203.
KCNQ4, a novel potassium channel expressed in sensory outer hair cells, is mutated in dominant deafness., Kubisch C,Schroeder BC,Friedrich T,Lütjohann B,El-Amraoui A,Marlin S,Petit C,Jentsch TJ, Cell. February 5, 1999; 96(3):1097-4172.
GJB2 mutations in Mongolia: complex alleles, low frequency, and reduced fitness of the deaf., Tekin M,Xia XJ,Erdenetungalag R,Cengiz FB,White TW,Radnaabazar J,Dangaasuren B,Tastan H,Nance WE,Pandya A, Ann Hum Genet. March 1, 2010; 74(2):1469-1809.