A novel de novo STXBP1 mutation is associated with mitochondrial complex I deficiency and late-onset juvenile-onset parkinsonism
Titel:
A novel de novo STXBP1 mutation is associated with mitochondrial complex I deficiency and late-onset juvenile-onset parkinsonism
Auteur:
Keogh, Michael J. Daud, D. Pyle, A. Duff, J. Griffin, H. He, L. Alston, C. L. Steele, H. Taggart, S. Basu, A. P. Taylor, R. W. Horvath, R. Ramesh, V. Chinnery, Patrick F.