A novel de novo STXBP1 mutation is associated with mitochondrial complex I deficiency and late-onset juvenile-onset parkinsonism
Crossref DOI link: https://doi.org/10.1007/s10048-014-0431-z
Published Online: 2014-11-25
Published Print: 2015-01
Update policy: https://doi.org/10.1007/springer_crossmark_policy
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.
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