Nancy Govea

Connexin-26 mutations in sporadic and inherited sensorineural deafness

Xavier Estivill, Paolo Fortina, Saul Surrey et al. · The Lancet · 1998 · 643 citations · Full text

Medicine, Genetics, Molecular Genetics +12

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

Xavier Estivill, Nancy Govea, Anna Barceló et al. · The American Journal of Human Genetics · 1998 · 549 citations · Full text

Life Sciences, Genetics, Molecular Genetics +13

Genetic landscape of 6089 inherited retinal dystrophies affected cases in Spain and their therapeutic and extended epidemiological implications

Irene Perea‐Romero, Gema Gordo, Ionut-Florin Iancu et al. · Scientific Reports · 2021 · 160 citations · Full text

Life Sciences, Genetics, Ophthalmology +16

The A1555G Mutation in the 12S rRNA Gene of Human mtDNA: Recurrent Origins and Founder Events in Families Affected by Sensorineural Deafness

Antonio Torroni, Fulvio Cruciani, Chiara Rengo et al. · The American Journal of Human Genetics · 1999 · 109 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

Linkage of DFNB1 to non-syndromic neurosensory autosomal-recessive deafness in Mediterranean families.

Paolo Gasparini, Xavier Estivill, Antonio Totaro et al. · PubMed · 1997 · 109 citations

Life Sciences, Genetics, Molecular Genetics +10