Two large French pedigrees with non syndromic sensorineural deafness and the mitochondrial DNA T7511C mutation: evidence for a modulatory factor-Reference-Cited by-同舟云学术

Two large French pedigrees with non syndromic sensorineural deafness and the mitochondrial DNA T7511C mutation: evidence for a modulatory factor

Published:2002-12 Issue:12 Volume:10 Page:851-856
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Chapiro Elise,Feldmann Delphine,Denoyelle Françoise,Sternberg Damien,Jardel Claude,Eliot Marie-Madeleine,Bouccara Didier,Weil Dominique,Garabédian Eréa-Noel,Couderc Rémy,Petit Christine,Marlin Sandrine

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://www.nature.com/articles/5200894.pdf

Reference15 articles.

1. Petit C, Levilliers J, Hardelin JP . Molecular genetics of hearing loss Annu Rev Genet 2001 35: 589–645

2. Tamagawa Y, Kitamura K, Hagiwara H et al. Audiologic findings in patients with a point mutation at nucleotide 3243 of mitochondrial DNA Ann Otol Rhinol Laryngol 1997 106: 338–342

3. Ballinger SW, Shoffner JM, Hedaya EV et al. Maternally transmitted diabetes and deafness associated with a 10.4 kb mitochondrial DNA deletion Nat Genet 1992 1: 11–15

4. Servior KB, Hatamochi A, Stewart IA et al. Mitochondrial A7445G mutation in two pedigrees with palmoplantar keratoderma and deafness Am J Med Genet 1998 75: 179–185

5. Jaber L, Shohat M, Bu X et al. Sensorineural deafness inherited as a tissue specific mitochondrial disorder J Med Genet 1992 29: 86–90

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