Dataset - Decoding complex inherited phenotypes in rare disorders: the DECIPHERD initiative for rare undiagnosed diseases in Chile

ISSN

1018-4813

Date Issued

2024

Author(s)

POLI HARLOWE, MARIA CECILIA BERTA

Facultad de Medicina Clínica Alemana Universidad del Desarrollo

REBOLLEDO JARAMILLO, BORIS EDUARDO

Facultad de Medicina Clínica Alemana Universidad del Desarrollo

CATALINA DEL PILAR LAGOS CARRILLO

Facultad de Medicina Clínica Alemana Universidad del Desarrollo

LUZ MARIA MARTIN CORTES

Facultad de Medicina Clínica Alemana Universidad del Desarrollo

Project(s)

Contribution of intergenerational mitonuclear mismatch to disease in Latin-American admixed patients.

SOLVING THE UNSOLVED: AN INTERDISCIPLINARY EVALUATION OF PERSONAL, SOCIAL AND HEALTH SYSTEM EFFECTS OF THE USE OF GENOMIC STRATEGIES FOR RARE UNDIAGNOSED DISORDERS

Functional genomics in autoinflammatory diseases

Advancing discoveries on rare disordes through international collaboration

Publication(s)

Decoding complex inherited phenotypes in rare disorders: the DECIPHERD initiative for rare undiagnosed diseases in Chile