Acute Infantile Liver Failure Due to Mutations in the TRMU Gene
Avraham Zeharia(Tel Aviv University), Orly Elpeleg(Hadassah Medical Center), Ann Saada(Jerusalem College of Technology), Daphna Marom(Tel Aviv University), Ivan Tarassov(Génétique Moléculaire Génomique Microbiologie), Noa Ofek(Hadassah Medical Center), Olga Karicheva(Génétique Moléculaire Génomique Microbiologie), Avraham Shaag(Shaare Zedek Medical Center), Reeval Segel(Shaare Zedek Medical Center), Hanna Mandel(Rambam Health Care Campus), Anne-Marie Mager-Heckel(Génétique Moléculaire Génomique Microbiologie), Marine Beinat(Hôpital Necker-Enfants Malades), Orit Pappo(Hadassah Medical Center), Agnès Rötig
Cited by 227
Related Papers
Persistent mitochondrial dysfunction and perinatal exposure to antiretroviral nucleoside analogues
|The Lancet|1999|667
Mutant mitochondrial thymidine kinase in mitochondrial DNA depletion myopathy
|Nature Genetics|2001|618
The deoxyguanosine kinase gene is mutated in individuals with depleted hepatocerebral mitochondrial DNA
|Nature Genetics|2001|584
Deleterious Mutation in the Mitochondrial Arginyl–Transfer RNA Synthetase Gene Is Associated with Pontocerebellar Hypoplasia
|The American Journal of Human Genetics|2007|331
Deficiency of the ADP-Forming Succinyl-CoA Synthase Activity Is Associated with Encephalomyopathy and Mitochondrial DNA Depletion
|The American Journal of Human Genetics|2005|313