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PedAM

Pediatric Disease Annotations & Medicines




Disease wolfram syndrome
Phenotype C0878544|cardiomyopathy
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.

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