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Alston, C.L.* ; Veling, M.T.* ; Heidler, J.* ; Taylor, L.S.* ; He, L.* ; Broomfield, A.* ; Pavaine, J.* ; Prokisch, H. ; Wortmann, S.B. ; Bonnen, P.E.* ; McFarland, R.* ; Wittig, I.* ; Pagliarini, D.J.* ; Taylor, R.W.*

Mutations in NDUFAF8 cause Leigh syndrome with an isolated complex I deficiency.

Eur. J. Hum. Genet. 27, 861-861 (2019)
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Publication type Article: Journal article
Document type Meeting abstract
Corresponding Author
ISSN (print) / ISBN 1018-4813
e-ISSN 1476-5438
Journal European Journal of Human Genetics
Quellenangaben Volume: 27, Issue: , Pages: 861-861 Article Number: , Supplement: ,
Publisher Nature Publishing Group
Publishing Place Macmillan Building, 4 Crinan St, London N1 9xw, England
Non-patent literature Publications
Reviewing status Peer reviewed
Institute(s) Institute of Human Genetics (IHG)