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Frontiers in Molecular Neuroscience|January 10, 2018
DFNB1 Non-syndromic Hearing Impairment: Diversity of Mutations and Associated PhenotypesFrancisco J Del Castillo, Ignacio Del CastilloFrontiers in Bioscience (Landmark Edition)|May 31, 2011
The DFNB1 subtype of autosomal recessive non-syndromic hearing impairmentFrancisco J del Castillo, Ignacio del CastilloFrontiers in Bioscience (Landmark Edition)|December 29, 2011
Genetics of isolated auditory neuropathiesFrancisco J Del Castillo, Ignacio Del CastilloHearing Research|July 19, 2015
Audibility, speech perception and processing of temporal cues in ribbon synaptic disorders due to OTOF mutationsRosamaria Santarelli, Ignacio del Castillo, Elona Cama, et al.Human Genetics|January 19, 2022
Genetic etiology of non-syndromic hearing loss in EuropeIgnacio Del Castillo, Matías Morín, María Domínguez-Ruiz, et al.Genes|April 3, 2021
A Novel Truncating Mutation in HOMER2 Causes Nonsyndromic Progressive DFNA68 Hearing Loss in a Spanish FamilyMaría Lachgar, Matías Morín, Manuela Villamar, et al.Audiology Research|December 23, 2021
Electrocochleography in Auditory Neuropathy Related to Mutations in the OTOF or OPA1 GeneRosamaria Santarelli, Pietro Scimemi, Chiara La Morgia, et al.International Journal of Pediatric Otorhinolaryngology|September 12, 2024
Hearing loss secondary to variants in the OTOF geneCarmelo Morales-Angulo, Jaime Gallo-Terán, Rocío González-Aguado, et al.Genetic Testing and Molecular Biomarkers|January 16, 2010
Hypothesizing an ancient Greek origin of the GJB2 35delG mutation: can science meet history?Haris Kokotas, Maria Grigoriadou, Manuela Villamar, et al.Pageof 7