Familial Progressive Sensorineural Deafness Is Mainly Due to the mtDNA A1555G Mutation and Is Enhanced by Treatment with Aminoglycosides
The American Journal of Human Genetics1998Vol. 62(1), pp. 27–35
Citations Over TimeTop 1% of 1998 papers
Xavier Estivill, Nancy Govea, Anna Barceló, E Perelló, Célia Bádenas, E. herrera romero, Luis Moral, Rosaria Scozzari, Leila D'Urbano, Massimo Zeviani, Antonio Torroni
Related Papers
- → Effect of N‐acetyl‐cysteine treatment on sensorineural hearing loss: a meta‐analysis(2021)29 cited
- → Osteogenesis imperfecta: the audiological phenotype lacks correlation with the genotype(2011)64 cited
- → KMT2D Deficiency Causes Sensorineural Hearing Loss in Mice and Humans(2023)2 cited
- → Characterization of hearing loss in pediatric patients with osteogenesis imperfecta(2024)1 cited
- → Molecular bases of hearing loss in multi-systemic mitochondrial cytopathy(2006)10 cited