Non-Syndromic Autosomal Dominant Hearing Loss: The First Italian Family Carrying a Mutation in the NCOA3 Gene

por Tesolin, Paola, Morgan, Anna, Notarangelo, Michela, Ortore, Rocco Pio, Concas, Maria Pina, Notarangelo, Angelantonio, Girotto, Giorgia
Publicado 2021

Compound Heterozygosity for OTOA Truncating Variant and Genomic Rearrangement Cause Autosomal Recessive Sensorineural Hearing Loss in an Italian Family

por Ortore, Rocco Pio, Leone, Maria Pia, Palumbo, Orazio, Petracca, Antonio, Trecca, Eleonora M. C., D’Ecclesia, Aurelio, Vigliaroli, Ciro Lucio, Micale, Lucia, Longo, Francesco, Melchionda, Salvatore, Castori, Marco
Publicado 2021