Co-existence of frataxin and cardiac troponin T gene mutations in a child with Friedreich Ataxia and familial hypertrophic cardiomyopathy

Human mutation

Volumn 19, Issue 3, 2002, Pages 309-310

  Cuda, Giovanni ^a   Mussari, Andrea ^a   Concolino, Daniela ^a   Costanzo, Francesco S ^a   Strisciuglio, Pietro ^a  

^a UNIVERSITY MAGNA GRAECIA OF CATANZARO   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

FRATAXIN; IRON BINDING PROTEIN; PHOSPHOTRANSFERASE; TROPONIN T;

ARTICLE; CASE REPORT; CHONDRODYSPLASIA; DIFFERENTIAL DIAGNOSIS; ECHOCARDIOGRAPHY; ELECTROCARDIOGRAPHY; FEMALE; FRIEDREICH ATAXIA; GENETICS; HUMAN; HYPERTROPHIC CARDIOMYOPATHY; MALE; MUTATION; NUCLEOTIDE SEQUENCE; PEDIGREE; PRESCHOOL CHILD;

CARDIOMYOPATHY, HYPERTROPHIC; CHILD, PRESCHOOL; DIAGNOSIS, DIFFERENTIAL; DNA MUTATIONAL ANALYSIS; ECHOCARDIOGRAPHY; ELECTROCARDIOGRAPHY; FEMALE; FRIEDREICH ATAXIA; HUMANS; IRON-BINDING PROTEINS; MALE; MUTATION; OSTEOCHONDRODYSPLASIAS; PEDIGREE; PHOSPHOTRANSFERASES (ALCOHOL GROUP ACCEPTOR); TROPONIN T;

EID: 0036517116     PISSN: None     EISSN: 10981004     Source Type: Journal    
DOI: 10.1002/humu.9019     Document Type: Article

References (0)