Portal de investigación
Inherited hearing loss: from molecular mechanisms to personalized therapies.
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INSTITUTO DE SALUD CARLOS III
Resultados del Ensayo Clínico
Clinical, Genetic, Morphological and Functional Correlations in a Large Series of Patients with Primary Ciliary Dyskinesia: A Heterogeneous Disease with a Controversial Diagnosis
Carretero-Vilarroig, L; (...); Jaijo, T
Article. 10.1007/s40291-025-00801-w. 2025
Outcomes of a Pilot Newborn Screening Program for Spinal Muscular Atrophy in the Valencian Community
Berzal-Serrano, A; (...); Millán, JM
Article. 10.3390/ijns11010007. 2025
Cita
Inherited hearing loss: from molecular mechanisms to personalized therapies. (CP22/00028). INSTITUTO DE SALUD CARLOS III. 2023-2027. IP:GEMA GARCÍA GARCÍA.