TIM13/YGR181W Literature Guide Help

Other names published for TIM13: YGR181W

TIM13 - Disease Gene Related (4)

ReferenceOther Genes Addressed
Roesch K, et al.  (2004) The calcium-binding aspartate/glutamate carriers, citrin and aralar1, are new substrates for the DDP1/TIMM8a-TIMM13 complex. Hum Mol Genet 13(18):2101-11
Hofmann S, et al.  (2002) The C66W mutation in the deafness dystonia peptide 1 (DDP1) affects the formation of functional DDP1.TIM13 complexes in the mitochondrial intermembrane space. J Biol Chem 277(26):23287-93
Rothbauer U, et al.  (2001) Role of the deafness dystonia peptide 1 (DDP1) in import of human Tim23 into the inner membrane of mitochondria. J Biol Chem 276(40):37327-34
Koehler CM, et al.  (1999) Human deafness dystonia syndrome is a mitochondrial disease. Proc Natl Acad Sci U S A 96(5):2141-6