Citations for
1CTMHD, GFER
Structure of the human sulfhydryl oxidase augmenter of liver regeneration and characterization of a human mutation causing an autosomal recessive myopathy .
Daithankar VN, Schaefer SA, Dong M, Bahnson BJ, Thorpe C.
Biochemistry 49(31):6737-45.PMID: 20593814 2010
2CTMHD, GFER
The mitochondrial disulfide relay system protein GFER is mutated in autosomal-recessive myopathy with cataract and combined respiratory-chain deficiency.
Di Fonzo A, Ronchi D, Lodi T, Fassone E, Tigano M, Lamperti C, Corti S, Bordoni A, Fortunato F, Nizzardo M, Napoli L, Donadoni C, Salani S, Saladino F, Moggio M, Bresolin N, Ferrero I, Comi GP.
Am J Hum Genet 84(5):594-604. Epub 2009 Apr 30. 2009