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B.02 Recessive mutations in ATP8A2 cause severe hypotonia, ..:

McMillan, HJ ; Telegrafi, A ; Singleton, A...
Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 45 (2018) s2 - p. S12-S12 , 2018

Link: https://doi.org/10.1017/cjn.2018.90

RT Journal
T1 <Title>B.02 Recessive mutations in ATP8A2 cause severe hypotonia, cognitive impairment, hyperkinetic movement disorders and progressive optic atrophy</Title>

UL https://suche.suub.uni-bremen.de/peid=cr-10.1017_cjn.2018.90&Exemplar=1&LAN=DE
				
A1 McMillan, HJ
A1 Telegrafi, A
A1 Singleton, A
A1 Cho, M
A1 Lelli, D
A1 Lynn, FC
A1 Griffin, J
A1 Asamoah, A
A1 Rinne, T
A1 Erasmus, CE
A1 Koolen, DA
A1 Haaxma, CA
A1 Keren, B
A1 Doummar, D
A1 Mignot, C
A1 Thompson, I
A1 Velsher, L
A1 Dehghani, M
A1 Vahidi Mehrjardi, M
A1 Maroofian, R
A1 Tchan, M
A1 Simons, C
A1 Christodoulou, J
A1 Martín-Hernández, E
A1 Guillen Sacoto, MJ
A1 Henderson, LB
A1 McLaughlin, H
A1 Molday, LL
A1 Molday, RS
A1 Yoon, G
PB Cambridge University Press (CUP)
YR 2018
SN 0317-1671
SN 2057-0155
JF Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques
VO 45
IS s2
SP S12
OP S12
LK http://dx.doi.org/https://doi.org/10.1017/cjn.2018.90
DO https://doi.org/10.1017/cjn.2018.90
SF ELIB - SuUB Bremen

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