PubMed (OMIM) for id: 436997

Year	Number of Results
1966	1
1994	1
1995	1
1997	2
1998	2
1999	4
2000	3
2001	1
2002	1
2024	0

1

A mutational hot spot in the KCNQ4 gene responsible for autosomal dominant hearing impairment.

Van Camp G, Coucke PJ, Akita J, Fransen E, Abe S, De Leenheer EM, Huygen PL, Cremers CW, Usami S. Van Camp G, et al. Hum Mutat. 2002 Jul;20(1):15-9. doi: 10.1002/humu.10096. Hum Mutat. 2002. PMID: 12112653

2

Clinical and genetic features of nonsyndromic autosomal dominant sensorineural hearing loss: KCNQ4 is a gene responsible in Japanese.

Akita J, Abe S, Shinkawa H, Kimberling WJ, Usami S. Akita J, et al. J Hum Genet. 2001;46(7):355-61. doi: 10.1007/s100380170053. J Hum Genet. 2001. PMID: 11450843

3

Mutations in the KCNQ4 K+ channel gene, responsible for autosomal dominant hearing loss, cluster in the channel pore region.

Van Hauwe P, Coucke PJ, Ensink RJ, Huygen P, Cremers CW, Van Camp G. Van Hauwe P, et al. Am J Med Genet. 2000 Jul 31;93(3):184-7. doi: 10.1002/1096-8628(20000731)93:3<184::aid-ajmg4>3.0.co;2-5. Am J Med Genet. 2000. PMID: 10925378

4

KCNQ4, a K+ channel mutated in a form of dominant deafness, is expressed in the inner ear and the central auditory pathway.

Kharkovets T, Hardelin JP, Safieddine S, Schweizer M, El-Amraoui A, Petit C, Jentsch TJ. Kharkovets T, et al. Proc Natl Acad Sci U S A. 2000 Apr 11;97(8):4333-8. doi: 10.1073/pnas.97.8.4333. Proc Natl Acad Sci U S A. 2000. PMID: 10760300 Free PMC article.

5

Mutant ion channel in cochlear hair cells causes deafness.

Trussell L. Trussell L. Proc Natl Acad Sci U S A. 2000 Apr 11;97(8):3786-8. doi: 10.1073/pnas.97.8.3786. Proc Natl Acad Sci U S A. 2000. PMID: 10760249 Free PMC article. No abstract available.

6

Novel mutation in the KCNQ4 gene in a large kindred with dominant progressive hearing loss.

Talebizadeh Z, Kelley PM, Askew JW, Beisel KW, Smith SD. Talebizadeh Z, et al. Hum Mutat. 1999;14(6):493-501. doi: 10.1002/(SICI)1098-1004(199912)14:6<493::AID-HUMU8>3.0.CO;2-P. Hum Mutat. 1999. PMID: 10571947

7

Mutations in the KCNQ4 gene are responsible for autosomal dominant deafness in four DFNA2 families.

Coucke PJ, Van Hauwe P, Kelley PM, Kunst H, Schatteman I, Van Velzen D, Meyers J, Ensink RJ, Verstreken M, Declau F, Marres H, Kastury K, Bhasin S, McGuirt WT, Smith RJ, Cremers CW, Van de Heyning P, Willems PJ, Smith SD, Van Camp G. Coucke PJ, et al. Hum Mol Genet. 1999 Jul;8(7):1321-8. doi: 10.1093/hmg/8.7.1321. Hum Mol Genet. 1999. PMID: 10369879

8

Deafness linked to DFNA2: one locus but how many genes?

Van Hauwe P, Coucke PJ, Declau F, Kunst H, Ensink RJ, Marres HA, Cremers CW, Djelantik B, Smith SD, Kelley P, Van de Heyning PH, Van Camp G. Van Hauwe P, et al. Nat Genet. 1999 Mar;21(3):263. doi: 10.1038/6778. Nat Genet. 1999. PMID: 10080176 No abstract available.

9

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. Kubisch C, et al. Cell. 1999 Feb 5;96(3):437-46. doi: 10.1016/s0092-8674(00)80556-5. Cell. 1999. PMID: 10025409 Free article.

10

Mutations in the gene encoding gap junction protein beta-3 associated with autosomal dominant hearing impairment.

Xia JH, Liu CY, Tang BS, Pan Q, Huang L, Dai HP, Zhang BR, Xie W, Hu DX, Zheng D, Shi XL, Wang DA, Xia K, Yu KP, Liao XD, Feng Y, Yang YF, Xiao JY, Xie DH, Huang JZ. Xia JH, et al. Nat Genet. 1998 Dec;20(4):370-3. doi: 10.1038/3845. Nat Genet. 1998. PMID: 9843210

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