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Biallelic Loss-of-Function Variants in AIMP1 Cause a Rare N..:
Accogli, Andrea
;
Guerrero, Kether
;
D'Agostino, Maria Daniela
...
Journal of Child Neurology. 34 (2018) 2 - p. 74-80 , 2018
Link:
https://doi.org/10.1177/0883073818811223
RT Journal T1
Biallelic Loss-of-Function Variants in AIMP1 Cause a Rare Neurodegenerative Disease
UL https://suche.suub.uni-bremen.de/peid=cr-10.1177_0883073818811223&Exemplar=1&LAN=DE A1 Accogli, Andrea A1 Guerrero, Kether A1 D'Agostino, Maria Daniela A1 Tran, Luan A1 Cieuta-Walti, Cécile A1 Thiffault, Isabelle A1 Chénier, Sébastien A1 Schwartzentruber, Jeremy A1 Majewski, Jacek A1 Bernard, Geneviève A1 Care4Rare Canada Consortium PB SAGE Publications YR 2018 SN 0883-0738 SN 1708-8283 JF Journal of Child Neurology VO 34 IS 2 SP 74 OP 80 LK http://dx.doi.org/https://doi.org/10.1177/0883073818811223 DO https://doi.org/10.1177/0883073818811223 SF ELIB - SuUB Bremen
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