Additional file 1: of Comprehensive genomic diagnosis of non-syndromic and syndromic hereditary hearing loss in Spanish patients
Year: 2018
Type: dataset
Abstract: List of phenotypes potentially related to hearing defects used as keywords for initial query on HGMD. (XLSX 16 kb)
Source: Figshare
Authors: Cabanillas, Rubén, Diñeiro, Marta, Cifuentes, Guadalupe, Castillo, David, Pruneda, Patricia, Álvarez, Rebeca, Sánchez-Durán, Noelia, Capín, Raquel, Plasencia, Ana, Viejo-Díaz, Mónica, García-González, Noelia, Hernando, Inés, Llorente, José, Repáraz-Andrade, Alfredo, Torreira-Banzas, Cristina, Rosell, Jordi, Govea, Nancy, Gómez-Martínez, Justo, Núñez-Batalla, Faustino, Garrote, José, Mazón-Gutiérrez, Ángel, Costales, María, Isidoro-García, María, García-Berrocal, Belén, Ordóñez, Gonzalo, Cadiñanos, Juan
Language: English
Subfield: Sensory Systems
Field: Neuroscience
Domain: Life Sciences
Open Access status: green
OpenAlex ID: W4394476554