Phenotypic variation of TTC19-deficient mitochondrial complex III deficiency: a case report and literature review.
Adelaide, Australia. In Am J Med Genet A, Jun 2015
It has been associated with mutations in MT-CYB, the only mitochondrial DNA encoded subunit, as well as in nine nuclear genes described thus far: BCS1L, TTC19, UQCRB, UQCRQ, UQCRC2, CYC1, UQCC2, LYRM7, and UQCC3.
Mutagenesis assays in yeast.
Atlanta, United States. In Methods, 2000
The assay for base substitution mutations uses a series of six strains with different mutations in one essential codon of the CYC1 gene.