TANGO2

Publications

Dines JN et al. TANGO2: expanding the clinical phenotype and spectrum of pathogenic variants. Genet Med. 2019;21(3):601-607. Erratum in: Genet Med. 2018 Oct 15;: PMID: 30245509.

Kremer LS et al. Bi-allelic Truncating Mutations in TANGO2 Cause Infancy-Onset Recurrent Metabolic Crises with Encephalocardiomyopathy. Am J Hum Genet. 2016;98(2):358-62. PMID: 26805782.

Lalani SR et al. Recurrent Muscle Weakness with Rhabdomyolysis, Metabolic Crises, and Cardiac Arrhythmia Due to Bi-allelic TANGO2 Mutations. Am J Hum Genet. 2016;98(2):347-57. PMID: 26805781.

Sen K et al. Homozygous TANGO2 Single Nucleotide Variants Presenting with Additional Manifestations Resembling Alternating Hemiplegia of Childhood-Expanding the Phenotype of a Recently Reported Condition. Neuropediatrics. 2019;50(2):122-125. PMID: 30650451.