Published in
Oxford University Press (OUP), Human Molecular Genetics, 4(27), p. 706-715
DOI: 10.1093/hmg/ddx436
Links
Tools
CHCHD10 mutations p.R15L and p.G66V cause motoneuron disease by haploinsufficiency
Journal article published in 2018 by
Sarah J. Brockmann,
Brockmann Sj,
Axel Freischmidt,
Patrick Oeckl 
,
Kathrin Müller,
Srinivas K. Ponna,
Anika M. Helferich,
Christoph Paone,
Ponna Sk,
Jörg Reinders ,
Kerstin Kojer,
Helferich Am,
Michael Orth,
Manu Jokela,
Mari Auranen
and other authors.
,
Kathrin Müller,
Srinivas K. Ponna,
Anika M. Helferich,
Christoph Paone,
Ponna Sk,
Jörg Reinders ,
Kerstin Kojer,
Helferich Am,
Michael Orth,
Manu Jokela,
Mari Auranen
and other authors.
This paper was not found in any repository, but could be made available legally by the author.
Full text: Unavailable
Published version:
archiving forbidden
Data provided by 