References
- Chen H, Thalmann I, Adams J C, Avraham K B, Copeland N G, Jenkins N A. CDNA cloning, tissue distribution, and chromosomal localization of Ocp2, a gene encoding a putative transcription-associated factor predominantly expressed in the auditory organs. Genomics 1995; 27: 389–98
- Fukushima K, Kasai N, Ueki Y, Nishizaki K, Sugata K, Hirakawa S. A gene for fluctuating, progressive autosomal dominant non-syndromic hearing impairment, DFNA16, maps to chromosome 2q23–24.3. Am J Human Genet
- Kubisch C, Schroeder B C, Friedrich T, Lutjohann B, El-Amraoui A, Marlin S. KCNQ4, a novel potassium channel expressed in sensory outer hair cells, is mutated in dominant deafness. Cell 1999; 96: 437–46
- Legan P K, Rau A, Keen J N, Richardson G P. The mouse tectorins. Modular matrix proteins of the inner ear homologous to components of the sperm-egg adhesion system. J Biol Chem 1997; 272: 8791–8801
- Probst F J, Fridell R A, Raphael Y, Saunders T L, Wang A, Liang Y. Correction of deafness in shaker-2 mice by an unconventional myosin in a BAC transgene. Science 1998; 280: 1444–7
- Thalmann I, Suszuki H, McCourt D W, Comegys T H, Thalmann R. Partial amino acid sequences of organ of Corti proteins OCP1 and OCP2 a progress report. Hearing Res 1993; 64: 191–8
- Verhoeven K, Van Laer L, Kirschhofer K, Legan P K, Hughes D C, Schatteman I. Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairment. Nat Genet 1998; 19: 60–2
- Wang A, Liang Y, Fridell R A, Probst F J, Wilcox E R, Touchman J W. Association of unconventional myosin MYO15 mutations with human nonsyndromic deafness DFNB3. Science 1998; 280: 1447–51
- Zbar R I, Ramesh A, Srisailapathy C R, Fukushima K, Wayne S, Smith R J. Passage to India: the search for genes causing autosomal recessive nonsyndromic hearing impairment. Otolaryngol Head Neck Surg 1998; 118: 333–7