PubMed (OMIM) for id: 371327

Year	Number of Results
1991	1
1993	1
1994	1
1996	1
1997	1
1998	1
1999	2
2001	2
2003	2
2005	1
2024	0

1

Targeted disruption of mouse Coch provides functional evidence that DFNA9 hearing loss is not a COCH haploinsufficiency disorder.

Makishima T, Rodriguez CI, Robertson NG, Morton CC, Stewart CL, Griffith AJ. Makishima T, et al. Hum Genet. 2005 Oct;118(1):29-34. doi: 10.1007/s00439-005-0001-4. Epub 2005 Oct 28. Hum Genet. 2005. PMID: 16078052

2

Mutations in the COCH gene are a frequent cause of autosomal dominant progressive cochleo-vestibular dysfunction, but not of Meniere's disease.

Usami S, Takahashi K, Yuge I, Ohtsuka A, Namba A, Abe S, Fransen E, Patthy L, Otting G, Van Camp G. Usami S, et al. Eur J Hum Genet. 2003 Oct;11(10):744-8. doi: 10.1038/sj.ejhg.5201043. Eur J Hum Genet. 2003. PMID: 14512963

3

Mutations in COCH that result in non-syndromic autosomal dominant deafness (DFNA9) affect matrix deposition of cochlin.

Grabski R, Szul T, Sasaki T, Timpl R, Mayne R, Hicks B, Sztul E. Grabski R, et al. Hum Genet. 2003 Oct;113(5):406-16. doi: 10.1007/s00439-003-0992-7. Epub 2003 Aug 20. Hum Genet. 2003. PMID: 12928864

4

Inner ear localization of mRNA and protein products of COCH, mutated in the sensorineural deafness and vestibular disorder, DFNA9.

Robertson NG, Resendes BL, Lin JS, Lee C, Aster JC, Adams JC, Morton CC. Robertson NG, et al. Hum Mol Genet. 2001 Oct 15;10(22):2493-500. doi: 10.1093/hmg/10.22.2493. Hum Mol Genet. 2001. PMID: 11709536

5

A common ancestor for COCH related cochleovestibular (DFNA9) patients in Belgium and The Netherlands bearing the P51S mutation.

Fransen E, Verstreken M, Bom SJ, Lemaire F, Kemperman MH, De Kok YJ, Wuyts FL, Verhagen WI, Huygen PL, McGuirt WT, Smith RJ, Van Maldergem LV, Declau F, Cremers CW, Van De Heyning PH, Cremers FP, Van Camp G. Fransen E, et al. J Med Genet. 2001 Jan;38(1):61-5. doi: 10.1136/jmg.38.1.61. J Med Genet. 2001. PMID: 11332404 Free PMC article. No abstract available.

6

High prevalence of symptoms of Menière's disease in three families with a mutation in the COCH gene.

Fransen E, Verstreken M, Verhagen WI, Wuyts FL, Huygen PL, D'Haese P, Robertson NG, Morton CC, McGuirt WT, Smith RJ, Declau F, Van de Heyning PH, Van Camp G. Fransen E, et al. Hum Mol Genet. 1999 Aug;8(8):1425-9. doi: 10.1093/hmg/8.8.1425. Hum Mol Genet. 1999. PMID: 10400989

7

A Pro51Ser mutation in the COCH gene is associated with late onset autosomal dominant progressive sensorineural hearing loss with vestibular defects.

de Kok YJ, Bom SJ, Brunt TM, Kemperman MH, van Beusekom E, van der Velde-Visser SD, Robertson NG, Morton CC, Huygen PL, Verhagen WI, Brunner HG, Cremers CW, Cremers FP. de Kok YJ, et al. Hum Mol Genet. 1999 Feb;8(2):361-6. doi: 10.1093/hmg/8.2.361. Hum Mol Genet. 1999. PMID: 9931344

8

Mutations in a novel cochlear gene cause DFNA9, a human nonsyndromic deafness with vestibular dysfunction.

Robertson NG, Lu L, Heller S, Merchant SN, Eavey RD, McKenna M, Nadol JB Jr, Miyamoto RT, Linthicum FH Jr, Lubianca Neto JF, Hudspeth AJ, Seidman CE, Morton CC, Seidman JG. Robertson NG, et al. Nat Genet. 1998 Nov;20(3):299-303. doi: 10.1038/3118. Nat Genet. 1998. PMID: 9806553

9

Mapping and characterization of a novel cochlear gene in human and in mouse: a positional candidate gene for a deafness disorder, DFNA9.

Robertson NG, Skvorak AB, Yin Y, Weremowicz S, Johnson KR, Kovatch KA, Battey JF, Bieber FR, Morton CC. Robertson NG, et al. Genomics. 1997 Dec 15;46(3):345-54. doi: 10.1006/geno.1997.5067. Genomics. 1997. PMID: 9441737

10

A gene for non-syndromic autosomal dominant progressive postlingual sensorineural hearing loss maps to chromosome 14q12-13.

Manolis EN, Yandavi N, Nadol JB Jr, Eavey RD, McKenna M, Rosenbaum S, Khetarpal U, Halpin C, Merchant SN, Duyk GM, MacRae C, Seidman CE, Seidman JG. Manolis EN, et al. Hum Mol Genet. 1996 Jul;5(7):1047-50. doi: 10.1093/hmg/5.7.1047. Hum Mol Genet. 1996. PMID: 8817345

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