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Genome sequencing in persistently unsolved white matter dis..:

Helman, Guy ; Lajoie, Bryan R. ; Crawford, Joanna...
Annals of Clinical and Translational Neurology. 7 (2020) 1 - p. 144-152 , 2020

Link: https://doi.org/10.1002/acn3.50957

RT Journal
T1 <Title>Genome sequencing in persistently unsolved white matter disorders</Title>

UL https://suche.suub.uni-bremen.de/peid=cr-10.1002_acn3.50957&Exemplar=1&LAN=DE
				
A1 Helman, Guy
A1 Lajoie, Bryan R.
A1 Crawford, Joanna
A1 Takanohashi, Asako
A1 Walkiewicz, Marzena
A1 Dolzhenko, Egor
A1 Gross, Andrew M.
A1 Gainullin, Vladimir G.
A1 Bent, Stephen J.
A1 Jenkinson, Emma M.
A1 Ferdinandusse, Sacha
A1 Waterham, Hans R.
A1 Dorboz, Imen
A1 Bertini, Enrico
A1 Miyake, Noriko
A1 Wolf, Nicole I.
A1 Abbink, Truus E. M.
A1 Kirwin, Susan M.
A1 Tan, Christina M.
A1 Hobson, Grace M.
A1 Guo, Long
A1 Ikegawa, Shiro
A1 Pizzino, Amy
A1 Schmidt, Johanna L.
A1 Bernard, Genevieve
A1 Schiffmann, Raphael
A1 van der Knaap, Marjo S.
A1 Simons, Cas
A1 Taft, Ryan J.
A1 Vanderver, Adeline
PB Wiley
YR 2020
SN 2328-9503
SN 2328-9503
JF Annals of Clinical and Translational Neurology
VO 7
IS 1
SP 144
OP 152
LK http://dx.doi.org/https://doi.org/10.1002/acn3.50957
DO https://doi.org/10.1002/acn3.50957
SF ELIB - SuUB Bremen

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