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Una nueva mutación en el gen CNGA3 causante de acromatopsia incompleta
A novel mutation in the CNGA3 gene responsible for incomplete achromatopsia
C. Burgueño-Montañés
, M. Colunga Cueva, C. Costales Álvarez
Autor para correspondencia
Servicio de Oftalmología, Hospital Universitario Central de Asturias, Oviedo, España
Leído
1626
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