Home Contact Sitemap

PedAM

Pediatric Disease Annotations & Medicines




Disease cerebellar degeneration
Phenotype C0917796|leber\'s hereditary optic neuropathy
Sentences 1
PubMedID- 23091534 leber's hereditary optic neuropathy with olivocerebellar degeneration due to g11778a and t3394c mutations in the mitochondrial dna.

Page: 1