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SPG7 mutations in amyotrophic lateral sclerosis: a genetic ..:
Osmanovic, Alma
;
Widjaja, Maylin
;
Förster, Alisa
...
https://repository.publisso.de/resource/frl:6469692. , 2020
Link:
https://repository.publisso.de/resource/frl:6469692
RT Journal T1
SPG7 mutations in amyotrophic lateral sclerosis: a genetic link to hereditary spastic paraplegia
UL https://suche.suub.uni-bremen.de/peid=base-ftzbmed:oai:frl.publisso.de:frl:6469692&Exemplar=1&LAN=DE A1 Osmanovic, Alma A1 Widjaja, Maylin A1 Förster, Alisa A1 Weder, Julia A1 Wattjes, Mike P A1 Lange, Inken A1 Sarikidi, Anastasia A1 Auber, Bernd A1 Raab, Peter A1 Christians, Anne A1 Preller, Matthias A1 Petri, Susanne A1 Weber, Ruthild G YR 2020 K1 Metalloendopeptidases/genetics [MeSH] K1 Mutation/genetics [MeSH] K1 Spastic Paraplegia K1 Hereditary/diagnostic imaging [MeSH] K1 Amyotrophic lateral sclerosis K1 SPG7 K1 Humans [MeSH] K1 Hereditary/genetics [MeSH] K1 Amyotrophic Lateral Sclerosis/diagnostic imaging [MeSH] K1 ATPases Associated with Diverse Cellular Activities/genetics [MeSH] K1 Motor neuron disease K1 Hereditary spastic paraplegia K1 Amyotrophic Lateral Sclerosis/genetics [MeSH] K1 Whole-exome sequencing K1 Original Communication JF https://repository.publisso.de/resource/frl:6469692 LK http://dx.doi.org/https://repository.publisso.de/resource/frl:6469692 DO https://repository.publisso.de/resource/frl:6469692 SF ELIB - SuUB Bremen
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