Familial Progressive Sensorineural Deafness Is Mainly Due to the mtDNA A1555G Mutation and Is Enhanced by Treatment with Aminoglycosides

Author:

Estivill Xavier,Govea Nancy,Barceló Anna,Perelló Enric,Badenas Cèlia,Romero Enrique,Moral Luis,Scozzari Rosaria,D'Urbano Leila,Zeviani Massimo,Torroni Antonio

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference37 articles.

1. N-methyl-D-aspartate antagonists limit aminoglycoside antibiotic-induced hearing loss;Basile;Nat Med,1996

2. Isolation of a candidate gene for Norrie disease by positional cloning;Berger;Nat Genet,1992

3. Genetic and environmental factors in profound prelingual deafness;Brown;Med Clin North Am,1969

4. Analysis of mtDNA variation in African populations reveals the most ancient of all human continent-specific haplogroups;Chen;Am J Hum Genet,1995

5. Epidemiology, etiology and genetic patterns;Cohen,1995

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