Ignacio Del Castillo

Madrid, MD, Spain

Last Updated: 09/26/2026

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Found 34 publications

DB-OTO Gene Therapy for Inherited Deafness.

DB-OTO Gene Therapy for Inherited Deafness.

Journal: The New England journal of medicine

Published: October 14, 2025

A Novel 1259 bp Intragenic Deletion in the GJB2 Gene in a Mexican Family with Congenital Profound Hearing Loss.

A Novel 1259 bp Intragenic Deletion in the GJB2 Gene in a Mexican Family with Congenital Profound Hearing Loss.

Journal: Audiology research

Published: June 18, 2025

De Novo Heterozygous GATA3 Missense Variant Causes an Unexpected Phenotype of Non-Syndromic Hearing Impairment with Apparently Recessive Inheritance.

De Novo Heterozygous GATA3 Missense Variant Causes an Unexpected Phenotype of Non-Syndromic Hearing Impairment with Apparently Recessive Inheritance.

Journal: International journal of molecular sciences

Published: May 23, 2025

Novel Cases of Non-Syndromic Hearing Impairment Caused by Pathogenic Variants in Genes Encoding Mitochondrial Aminoacyl-tRNA Synthetases.

Novel Cases of Non-Syndromic Hearing Impairment Caused by Pathogenic Variants in Genes Encoding Mitochondrial Aminoacyl-tRNA Synthetases.

Journal: Genes

Published: June 24, 2024

Sensorineural Hearing Loss in Patients With the m.1555A>G Mutation in the MTRNR1 Gene.

Sensorineural Hearing Loss in Patients With the m.1555A>G Mutation in the MTRNR1 Gene.

Journal: The Laryngoscope

Published: May 15, 2024

Hearing loss secondary to variants in the OTOF gene.

Hearing loss secondary to variants in the OTOF gene.

Journal: International journal of pediatric otorhinolaryngology

Published: April 04, 2024

A murine model for the del(GJB6-D13S1830) deletion recapitulating the phenotype of human DFNB1 hearing impairment: generation and functional and histopathological study.

A murine model for the del(GJB6-D13S1830) deletion recapitulating the phenotype of human DFNB1 hearing impairment: generation and functional and histopathological study.

Journal: BMC genomics

Published: February 06, 2024

Novel Pathogenic Variants in the Gene Encoding Stereocilin (STRC) Causing Non-Syndromic Moderate Hearing Loss in Spanish and Argentinean Subjects.

Novel Pathogenic Variants in the Gene Encoding Stereocilin (STRC) Causing Non-Syndromic Moderate Hearing Loss in Spanish and Argentinean Subjects.

Journal: Biomedicines

Published: October 10, 2023

Preservation of Distortion Product Otoacoustic Emissions in OTOF -Related Hearing Impairment.

Preservation of Distortion Product Otoacoustic Emissions in OTOF -Related Hearing Impairment.

Journal: Ear and hearing

Published: September 07, 2023

Thalamic Foxp2 regulates output connectivity and sensory-motor impairments in a model of Huntington's Disease.

Thalamic Foxp2 regulates output connectivity and sensory-motor impairments in a model of Huntington's Disease.

Journal: Cellular and molecular life sciences : CMLS

Published: May 04, 2023

Genetic Evaluation of Prelingual Hearing Impairment: Recommendations of an European Network for Genetic Hearing Impairment.

Genetic Evaluation of Prelingual Hearing Impairment: Recommendations of an European Network for Genetic Hearing Impairment.

Journal: Audiology research

Published: January 18, 2023

Postnatal Foxp2 regulates early psychiatric-like phenotypes and associated molecular alterations in the R6/1 transgenic mouse model of Huntington's disease.

Postnatal Foxp2 regulates early psychiatric-like phenotypes and associated molecular alterations in the R6/1 transgenic mouse model of Huntington's disease.

Journal: Neurobiology of disease

Published: May 06, 2022

Showing 1-12 of 34

Last Updated: 09/26/2026