Citations for
1DFNB18B, OTOG
Mutations of the gene encoding otogelin are a cause of autosomal-recessive nonsyndromic moderate hearing impairment.
Schraders M, Ruiz-Palmero L, Kalay E, Oostrik J, Del Castillo FJ, Sezgin O, Beynon AJ, Strom TM, Pennings RJ, Seco CZ, Oonk AM, Kunst HP, Domínguez-Ruiz M, García-Arumi AM, Del Campo M, Villamar M, Hoefsloot LH, Moreno F, Admiraal RJ, Del Castillo I, Kremer H.
Am J Hum Genet 91(5):883-9. doi: 10.1016/j.ajhg.2012.09.012. 2012
2DFNB84B, OTOG, OTOGL
Mutations in OTOGL, Encoding the Inner Ear Protein Otogelin-like, Cause Moderate Sensorineural Hearing Loss.
Yariz KO, Duman D, Seco CZ, Dallman J, Huang M, Peters TA, Sirmaci A, Lu N, Schraders M, Skromne I, Oostrik J, Diaz-Horta O, Young JI, Tokgoz-Yilmaz S, Konukseven O, Shahin H, Hetterschijt L, Kanaan M, Oonk AM, Edwards YJ, Li H, Atalay S, Blanton S, Desmidt AA, Liu XZ, Pennings RJ, Lu Z, Chen ZY, Kremer H, Tekin M.
Am J Hum Genet 91(5):872-82. doi: 10.1016/j.ajhg.2012.09.011. 2012
3OTOG
Spatiotemporal expression of otogelin in the developing and adult mouse inner ear.
El-Amraoui A, Cohen-Salmon M, Petit C, Simmler MC.
Hear Res 158(1-2):151-9. 2001
4OTOG
Twister mutant mice are defective for otogelin, a component specific to inner ear acellular membranes.
Simmler MC, Zwaenepoel I, Verpy E, Guillaud L, Elbaz C, Petit C, Panthier JJ.
Mamm Genome 11(11):960-6. 2000
5OTOG
Targeted disruption of otog results in deafness and severe imbalance.
Simmler MC, Cohen-Salmon M, El-Amraoui A, Guillaud L, Benichou JC, Petit C, Panthier JJ.
Nat Genet 24(2):139-43. 2000
6OTOG
Mapping of the otogelin gene (OTGN) to mouse chromosome 7 and human chromosome 11p14.3: a candidate for human autosomal recessive nonsyndromic deafness DFNB18.
Cohen-Salmon M, Mattei MG, Petit C.
Mamm Genome. 10(5):520-2. 1999
7OTOG
Otogelin: a glycoprotein specific to the acellular membranes of the inner ear.
Cohen-Salmon M, El-Amraoui A, Leibovici M, Petit C.
Proc Natl Acad Sci U S A 94(26):14450-5. 1997