Mitochondrial DNA mutations in patients with postlingual, nonsyndromic hearing impairment-Reference-Cited by-同舟云学术

Mitochondrial DNA mutations in patients with postlingual, nonsyndromic hearing impairment

Published:2004-08-04 Issue:1 Volume:13 Page:26-33
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Jacobs Howard T,Hutchin Timothy P,Käppi Timo,Gillies Greta,Minkkinen Kia,Walker John,Thompson Karen,Rovio Anja T,Carella Massimo,Melchionda Salvatore,Zelante Leopoldo,Gasparini Paolo,Pyykkö Ilmari,Shah Zahid H,Zeviani Massimo,Mueller Robert F

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://www.nature.com/articles/5201250.pdf

Reference46 articles.

1. Prezant TR, Agapian JV, Bohlman MC et al: Mitochondrial ribosomal RNA mutation associated with both antibiotic-induced and non-syndromic deafness. Nat Genet 1993; 4: 289–294.

2. Reid FM, Vernham GA, Jacobs HT : A novel mitochondrial point mutation in a maternal pedigree with sensorineural deafness. Hum Mutat 1994; 3: 243–247.

3. Fischel-Ghodsian N, Prezant TR, Fournier P, Stewart IA, Maw M : Mitochondrial mutation associated with nonsyndromic deafness. Am J Otolaryngol 1995; 16: 403–408.

4. Tiranti V, Chariot P, Carella F et al: Maternally inherited hearing loss, ataxia and myoclonus associated with a novel point mutation in mitochondrial tRNASer(UCN) gene. Hum Mol Genet 1995; 4: 1421–1427.

5. Verhoeven K, Ensink RJ, Tiranti V et al: Hearing impairment and neurological dysfunction associated with a mutation in the mitochondrial tRNASer(UCN) gene. Eur J Hum Genet 1999; 7: 45–51.

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