IDENTIFICATION OF CONGENITAL DEAFNESS MUTATIONS IN CHILE
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Fecha de publicación: | 2018 |
Objetivos: | The main goal of this project was to describe the prevalence of the main mutations causing hearing loss of genetic origin in the Chilean population and to characterize the phenotype of possible new mutations in the GJB2 gene. |
Instrumento: | FONIS |
Año de Inicio/Término: | 2018-2022 |
Financiamiento/Sponsor: | CONICYT |
Rol del Usuario: | DIRECTOR(A) |
DOI: |
SA18I0194 |