PubMed (OMIM) for id: 9750

Year	Number of Results
1997	2
1999	1
2000	1
2005	1
2006	1
2007	1
2014	1
2016	1
2020	1
2024	0

1

A RIPOR2 in-frame deletion is a frequent and highly penetrant cause of adult-onset hearing loss.

de Bruijn SE, Smits JJ, Liu C, Lanting CP, Beynon AJ, Blankevoort J, Oostrik J, Koole W, de Vrieze E, Cremers CWRJ, Cremers FPM, Roosing S, Yntema HG, Kunst HPM, Zhao B, Pennings RJE, Kremer H; DOOFNL Consortium. de Bruijn SE, et al. J Med Genet. 2020 Jul 6:jmedgenet-2020-106863. doi: 10.1136/jmedgenet-2020-106863. Online ahead of print. J Med Genet. 2020. PMID: 32631815 Free PMC article.

2

Murine Fam65b forms ring-like structures at the base of stereocilia critical for mechanosensory hair cell function.

Zhao B, Wu Z, Müller U. Zhao B, et al. Elife. 2016 Jun 8;5:e14222. doi: 10.7554/eLife.14222. Elife. 2016. PMID: 27269051 Free PMC article.

3

FAM65B is a membrane-associated protein of hair cell stereocilia required for hearing.

Diaz-Horta O, Subasioglu-Uzak A, Grati M, DeSmidt A, Foster J 2nd, Cao L, Bademci G, Tokgoz-Yilmaz S, Duman D, Cengiz FB, Abad C, Mittal R, Blanton S, Liu XZ, Farooq A, Walz K, Lu Z, Tekin M. Diaz-Horta O, et al. Proc Natl Acad Sci U S A. 2014 Jul 8;111(27):9864-8. doi: 10.1073/pnas.1401950111. Epub 2014 Jun 23. Proc Natl Acad Sci U S A. 2014. PMID: 24958875 Free PMC article.

4

C6ORF32 is upregulated during muscle cell differentiation and induces the formation of cellular filopodia.

Yoon S, Molloy MJ, Wu MP, Cowan DB, Gussoni E. Yoon S, et al. Dev Biol. 2007 Jan 1;301(1):70-81. doi: 10.1016/j.ydbio.2006.11.002. Epub 2006 Nov 7. Dev Biol. 2007. PMID: 17150207 Free PMC article.

5

Fine mapping of autosomal dominant nonsyndromic hearing impairment DFNA21 to chromosome 6p24.1-22.3.

de Brouwer AP, Kunst HP, Krebsova A, van Asseldonk K, Reis A, Snoeckx RL, Van Camp G, Cremers CW, Cremers FP, Kremer H. de Brouwer AP, et al. Am J Med Genet A. 2005 Aug 15;137(1):41-6. doi: 10.1002/ajmg.a.30844. Am J Med Genet A. 2005. PMID: 16007628

6

Non-syndromal autosomal dominant hearing impairment: ongoing phenotypical characterization of genotypes.

Bom SJ, Kunst HP, Huygen PL, Cremers FP, Cremers CW. Bom SJ, et al. Br J Audiol. 1999 Oct;33(5):335-48. doi: 10.3109/03005369909090117. Br J Audiol. 1999. PMID: 10890148

7

Non-syndromic autosomal dominant progressive non-specific mid-frequency sensorineural hearing impairment with childhood to late adolescence onset (DFNA21).

Kunst H, Marres H, Huygen P, van Duijnhoven G, Krebsova A, van der Velde S, Reis A, Cremers F, Cremers C. Kunst H, et al. Clin Otolaryngol Allied Sci. 2000 Feb;25(1):45-54. doi: 10.1046/j.1365-2273.2000.00327.x. Clin Otolaryngol Allied Sci. 2000. PMID: 10764236

8

Prediction of the coding sequences of unidentified human genes. VII. The complete sequences of 100 new cDNA clones from brain which can code for large proteins in vitro.

Nagase T, Ishikawa K, Nakajima D, Ohira M, Seki N, Miyajima N, Tanaka A, Kotani H, Nomura N, Ohara O. Nagase T, et al. DNA Res. 1997 Apr 28;4(2):141-50. doi: 10.1093/dnares/4.2.141. DNA Res. 1997. PMID: 9205841 Free article.

9

PL48: a novel gene associated with cytotrophoblast and lineage-specific HL-60 cell differentiation.

Dakour J, Li H, Morrish DW. Dakour J, et al. Gene. 1997 Feb 7;185(2):153-7. doi: 10.1016/s0378-1119(96)00587-2. Gene. 1997. PMID: 9055809

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