DFNB21.

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作者信息

Denoyelle Françoise, Mustapha Mirna, Petit Christine

机构信息

Unité de Génétique des Déficits Sensoriels, CNRS URA 1968, Institut Pasteur, Paris, France.

出版信息

Adv Otorhinolaryngol. 2002;61:153-5. doi: 10.1159/000066827.

DOI:10.1159/000066827

PMID:12408078

Abstract

摘要

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引用本文的文献

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相似文献

DFNB21.

Adv Otorhinolaryngol. 2002;61:153-5. doi: 10.1159/000066827.

Clinical presentation of DFNA8-DFNA12.

Adv Otorhinolaryngol. 2002;61:60-5. doi: 10.1159/000066805.

Distinctive audiometric profile associated with DFNB21 alleles of TECTA.

J Med Genet. 2003 May;40(5):360-3. doi: 10.1136/jmg.40.5.360.

Histopathology of nonsyndromic autosomal dominant midfrequency sensorineural hearing loss.

Otol Neurotol. 2008 Aug;29(5):601-6. doi: 10.1097/MAO.0b013e3181778245.

Audiological evaluation of affected members from a Dutch DFNA8/12 (TECTA) family.

J Assoc Res Otolaryngol. 2007 Mar;8(1):1-7. doi: 10.1007/s10162-006-0060-9. Epub 2006 Nov 30.

X-linked mixed deafness syndrome with congenital fixation of the stapedial footplate and perilymphatic gusher (DFN3).

Adv Otorhinolaryngol. 2002;61:161-7. doi: 10.1159/000066826.

Identification of three novel TECTA mutations in Iranian families with autosomal recessive nonsyndromic hearing impairment at the DFNB21 locus.

Am J Med Genet A. 2007 Jul 15;143A(14):1623-9. doi: 10.1002/ajmg.a.31718.

Two deaf mice, two deaf mice..

Nat Med. 1998 May;4(5):560-1. doi: 10.1038/nm0598-560.

An alpha-tectorin gene defect causes a newly identified autosomal recessive form of sensorineural pre-lingual non-syndromic deafness, DFNB21.

Hum Mol Genet. 1999 Mar;8(3):409-12. doi: 10.1093/hmg/8.3.409.

A novel TECTA mutation causes ARNSHL.

Int J Pediatr Otorhinolaryngol. 2017 Jan;92:88-93. doi: 10.1016/j.ijporl.2016.11.010. Epub 2016 Nov 15.

引用本文的文献

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Braz J Otorhinolaryngol. 2005 Mar-Apr;71(2):216-23. doi: 10.1016/s1808-8694(15)31313-6. Epub 2005 Aug 2.