Serre, V.

acad 9 mutation patient mitochondrial i activity ficiency activity protein flavin wild-type acad 9 wild-type ribo flavin analysis assembly function oxidative broblast phosphorylation brain fi broblasts study subunit region genet ribo flavin treatment scholte acad 9. disease control family institute hydrogen bond structure identi fied transduction defect c .1405c mutation exercise intolerance substitution cause i assembly acad 9 mutation model arginine netherland chain 210–219 downloaded sequence i function disorder muscle centre acad 9 gene change native-polyacrylamide gel electrophoresis acad 9 protein b-oxidation position 532trp identi mapping department smeets r transduced tryptophan netherlands department pcr product zebra fish exercise residue leigh syndrome arg 532 oxidative phosphorylation treatment c .380g alignment leigh restriction gerard