Condition: LIVER FAILURE, INFANTILE, TRANSIENT


rs118203990 in TRMU gene and LIVER FAILURE, INFANTILE, TRANSIENT PMID 19732863 2009 Acute infantile liver failure due to mutations in the TRMU gene.

PMID 23625533 2013 Mitochondrial Infantile Liver Disease due to TRMU Gene Mutations: Three New Cases.

PMID 25665837 2015 Hepatic Copper Accumulation: A Novel Feature in Transient Infantile Liver Failure Due to TRMU Mutations?

PMID 21931168 2011 Reversible infantile respiratory chain deficiency is a unique, genetically heterogenous mitochondrial disease.