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1 Ergebnisse
1
CHCHD10 mutations p.R15L and p.G66V cause motoneuron diseas..:
Brockmann, Sarah J
;
Freischmidt, Axel
;
Oeckl, Patrick
...
Human Molecular Genetics. 27 (2018) 4 - p. 706-715 , 2018
Link:
https://doi.org/10.1093/hmg/ddx436
RT Journal T1
CHCHD10 mutations p.R15L and p.G66V cause motoneuron disease by haploinsufficiency
UL https://suche.suub.uni-bremen.de/peid=cr-10.1093_hmg_ddx436&Exemplar=1&LAN=DE A1 Brockmann, Sarah J A1 Freischmidt, Axel A1 Oeckl, Patrick A1 Müller, Kathrin A1 Ponna, Srinivas K A1 Helferich, Anika M A1 Paone, Christoph A1 Reinders, Jörg A1 Kojer, Kerstin A1 Orth, Michael A1 Jokela, Manu A1 Auranen, Mari A1 Udd, Bjarne A1 Hermann, Andreas A1 Danzer, Karin M A1 Lichtner, Peter A1 Walther, Paul A1 Ludolph, Albert C A1 Andersen, Peter M A1 Otto, Markus A1 Kursula, Petri A1 Just, Steffen A1 Weishaupt, Jochen H PB Oxford University Press (OUP) YR 2018 SN 0964-6906 SN 1460-2083 JF Human Molecular Genetics VO 27 IS 4 SP 706 OP 715 LK http://dx.doi.org/https://doi.org/10.1093/hmg/ddx436 DO https://doi.org/10.1093/hmg/ddx436 SF ELIB - SuUB Bremen
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