Home Contact Sitemap

PedAM

Pediatric Disease Annotations & Medicines




Disease cardiomyopathy
Phenotype C0043207|wolfram syndrome
Sentences 1
PubMedID- 21723259 Our study reported a tunisian patient with clinical features of moderate wolfram syndrome associated with cardiomyopathy, in whom we detected the nd1 m.3337g>a mutation with mitochondrial multiple deletions.

Page: 1