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Piekutowska-Abramczuk, D.* ; Stenton, S. ; Gusic, M. ; Ciara, E.* ; Wagner, M. ; Haack, T.B. ; Claeys, K.G.* ; Schrod, L.* ; Nava, C.* ; Narayanan, V.* ; Jurkiewicz, D.* ; Halat-Wolska, P.* ; Pelc, M.* ; Chrzanowska, K.* ; Ploski, R.* ; Meitinger, T. ; Pronicki, M. ; Pronicka, E.* ; Prokisch, H.

Novel FDXR pathogenic variants expand the clinical spectrum related to human ferredoxin reductase defects.

Eur. J. Hum. Genet. 27, 172-173 (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: 172-173 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)