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Items: 10

1.

A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness.

Yasunaga S, Grati M, Cohen-Salmon M, El-Amraoui A, Mustapha M, Salem N, El-Zir E, Loiselet J, Petit C.

Nat Genet. 1999 Apr;21(4):363-9.

PMID:
10192385
2.

Mouse tales from Kresge: the deafness mouse.

Drury SS, Keats BJ.

J Am Acad Audiol. 2003 Aug;14(6):296-301. Review.

PMID:
14552423
3.

Mapping and cloning hereditary deafness genes.

Cremers FP, Bitner-Glindzicz M, Pembrey ME, Ropers HH.

Curr Opin Genet Dev. 1995 Jun;5(3):371-5. Review.

PMID:
7549433
4.

OTOF-Related Deafness.

Shearer AE, Smith RJH.

In: Pagon RA, Adam MP, Ardinger HH, Wallace SE, Amemiya A, Bean LJH, Bird TD, Ledbetter N, Mefford HC, Smith RJH, Stephens K, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2017.
2008 Feb 29 [updated 2015 Jul 30].

5.

Otoferlin: a multi-C2 domain protein essential for hearing.

Pangršič T, Reisinger E, Moser T.

Trends Neurosci. 2012 Nov;35(11):671-80. doi: 10.1016/j.tins.2012.08.002. Epub 2012 Sep 7. Review.

PMID:
22959777
6.

Ferlins: regulators of vesicle fusion for auditory neurotransmission, receptor trafficking and membrane repair.

Lek A, Evesson FJ, Sutton RB, North KN, Cooper ST.

Traffic. 2012 Feb;13(2):185-94. doi: 10.1111/j.1600-0854.2011.01267.x. Epub 2011 Sep 6. Review.

7.

The molecular genetics of inherited deafness--current and future applications.

Bussoli TJ, Steel KP.

J Laryngol Otol. 1998 Jun;112(6):523-30. Review. No abstract available.

PMID:
9764289
8.

Unconventional myosins, the basis for deafness in mouse and man.

Hasson T.

Am J Hum Genet. 1997 Oct;61(4):801-5. Review. No abstract available.

9.

Similarities between mice and humans with hereditary deafness.

Steel KP.

Ann N Y Acad Sci. 1991;630:68-79. Review. No abstract available.

PMID:
1952625
10.

The molecular genetics of inherited deafness--current knowledge and recent advances.

Hardisty RE, Fleming J, Steel KP.

J Laryngol Otol. 1998 May;112(5):432-7. Review. No abstract available.

PMID:
9747469

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