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1 Ergebnisse
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TMEM63C mutations cause mitochondrial morphology defects an..:
Tábara, L. C
;
Al-Salmi, F
;
Maroofian, R
...
https://academic.oup.com/brain/article-lookup/doi/10.1093/brain/awac123. , 2022
Link:
https://doi.org/10.1093/brain/awac123
RT Journal T1
TMEM63C mutations cause mitochondrial morphology defects and underlie hereditary spastic paraplegia
UL https://suche.suub.uni-bremen.de/peid=base-ftrde:oai:rde.dspace-express.com:11287_622553&Exemplar=1&LAN=DE A1 Tábara, L. C A1 Al-Salmi, F A1 Maroofian, R A1 Al-Futaisi, A. M A1 Al-Murshedi, F A1 Kennedy, J A1 Day, J. O A1 Courtin, T A1 Al-Khayat, A A1 Galedari, H A1 Mazaheri, N A1 Protasoni, M A1 Johnson, M A1 Leslie, J. S A1 Salter, C. G A1 Rawlins, L. E A1 Fasham, J A1 Al-Maawali, A A1 Voutsina, N A1 Charles, P A1 Harrold, L A1 Keren, B A1 Kunji, E. R. S A1 Vona, B A1 Jelodar, G A1 Sedaghat, A A1 Shariati, G A1 Houlden, H A1 Crosby, A. H A1 Prudent, J A1 Baple, E. L PB Oxford University Press YR 2022 K1 Endoplasmic Reticulum/genetics/metabolism K1 Humans K1 Mitochondria/genetics K1 Mutation/genetics K1 Proteins/genetics K1 *Spastic Paraplegia K1 Hereditary K1 Tmem63c K1 endoplasmic reticulum/ER K1 hereditary spastic paraplegia/HSP K1 mitochondria K1 mitochondria-ER contact sites/MERCs JF https://academic.oup.com/brain/article-lookup/doi/10.1093/brain/awac123 LK http://dx.doi.org/https://doi.org/10.1093/brain/awac123 DO https://doi.org/10.1093/brain/awac123 SF ELIB - SuUB Bremen
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