Skip to main content
American Journal of Human Genetics logoLink to American Journal of Human Genetics
. 2010 Feb 12;86(2):295. doi: 10.1016/j.ajhg.2010.01.020

Acute Infantile Liver Failure Due to Mutations in the TRMU Gene

Avraham Zeharia , Avraham Shaag, Orit Pappo, Anne-Marie Mager-Heckel, Ann Saada, Marine Beinat, Olga Karicheva, Hanna Mandel, Noa Ofek, Reeval Segel, Daphna Marom, Agnes Rötig, Ivan Tarassov, Orly Elpeleg
PMCID: PMC2820182

(American Journal of Human Genetics 85, 401–407; September 11, 2009)

At the end of the body text, after “predominantly when the onset is at 1–4 months of age.”, the following sentences should have been included: “Another Israeli infant of Yemenite-Jewish origin, who presented with transient liver failure during infancy, was previously reported by Lev et al.17 In view of the similar presentation and ethnic origin, this patient could represent the first reported case of TRMU deficiency.” The authors regret this error. The reference to Lev et al. is given below:

Reference

  • 17.Lev D., Gilad E., Leshinsky-Silver E., Houri S., Levine A., Saada A., Lerman-Sagie T. Reversible fulminant lactic acidosis and liver failure in an infant with hepatic cytochrome-c oxidase deficiency. J. Inherit. Metab. Dis. 2002;25:371–377. doi: 10.1023/a:1020195616081. [DOI] [PubMed] [Google Scholar]

Articles from American Journal of Human Genetics are provided here courtesy of American Society of Human Genetics

RESOURCES