Large-scale molecular analysis of hereditary hearing loss genes in argentinean
deaf patients: lookingfora needle in a haystack
Revista
Acceso abierto
Revista
CONICET Digital
Hereditary Hearing Loss (HHL) is a common trait affecting 1 in 2000 new born children. The presence of over 100 different genes involved in HHL, lead us to go on board with Whole Exome Sequencing (WES) in order to search...
Idioma eng
Acceso abiertoRuta libre sin proxy. Acceso recomendado cuando no hay suscripción activa.
Open Access