Homozygous missense mutation in UQCRC2 associated with severe encephalomyopathy, mitochondrial complex III assembly defect and activation of mitochondrial protein quality control
Titel:
Homozygous missense mutation in UQCRC2 associated with severe encephalomyopathy, mitochondrial complex III assembly defect and activation of mitochondrial protein quality control
Auteur:
Burska, Daniela Stiburek, Lukas Krizova, Jana Vanisova, Marie Martinek, Vaclav Sladkova, Jana Zamecnik, Josef Honzik, Tomas Zeman, Jiri Hansikova, Hana Tesarova, Marketa
Verschenen in:
Biochimica et Biophysica Acta. Molecular basis of disease