Mutation of the human mitochondrial phenylalanine-tRNA synthetase causes infantile-onset epilepsy and cytochrome c oxidase deficiency
Titel:
Mutation of the human mitochondrial phenylalanine-tRNA synthetase causes infantile-onset epilepsy and cytochrome c oxidase deficiency
Auteur:
Almalki, Abdulraheem Alston, Charlotte L. Parker, Alasdair Simonic, Ingrid Mehta, Sarju G. He, Langping Reza, Mojgan Oliveira, Jorge M.A. Lightowlers, Robert N. McFarland, Robert Taylor, Robert W. Chrzanowska-Lightowlers, Zofia M.A.
Verschenen in:
Biochimica et Biophysica Acta. Molecular basis of disease