Home Contact Sitemap

PedAM

Pediatric Disease Annotations & Medicines




Disease hypothyroidism
Phenotype C0751651|mitochondrial disorder
Sentences 1
PubMedID- 26053701 Infantile mitochondrial disorder associated with subclinical hypothyroidism is caused by a rare mitochondrial dna 8691a>g mutation: a case report.

Page: 1