A novel nonsense variant in the CENPP gene segregates in a Swiss family with autosomal dominant low-frequency sensorineural hearing loss
FI: 5,351
Tipo: Article
Artículo original
Año: 2022
Autores
Robles-Bolivar, P; Bachinger, D; Parra-Perez, AM; Roman-Naranjo, P; Escalera-Balsera, A; Gallego-Martinez, A; Eckhard, AH; Lopez-Escamez, JA
Revista
Título: EUROPEAN JOURNAL OF HUMAN GENETICS
Cuartil
- Q1