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1 Ergebnisse
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Novel NDUFA13 Mutations Associated with OXPHOS Deficiency a..:
Adrián González-Quintana
;
Inés García-Consuegra
;
Amaya Belanger-Quintana
...
https://www.mdpi.com/2073-4425/11/8/855. , 2020
Link:
https://doi.org/10.3390/genes11080855
RT Journal T1
Novel NDUFA13 Mutations Associated with OXPHOS Deficiency and Leigh Syndrome: A Second Family Report
UL https://suche.suub.uni-bremen.de/peid=base-ftdoajarticles:oai:doaj.org_article:e6a9d620d273412bbaf3ad94b456cc7d&Exemplar=1&LAN=DE A1 Adrián González-Quintana A1 Inés García-Consuegra A1 Amaya Belanger-Quintana A1 Pablo Serrano-Lorenzo A1 Alejandro Lucia A1 Alberto Blázquez A1 Jorge Docampo A1 Cristina Ugalde A1 María Morán A1 Joaquín Arenas A1 Miguel A. Martín PB MDPI AG YR 2020 K1 mitochondrial complex I deficiency K1 NDUFA13 gene K1 mitochondrial OXPHOS dysfunction K1 Leigh syndrome K1 OXPHOS assembly K1 OXPHOS diagnosis K1 Genetics K1 QH426-470 JF https://www.mdpi.com/2073-4425/11/8/855 LK http://dx.doi.org/https://doi.org/10.3390/genes11080855 DO https://doi.org/10.3390/genes11080855 SF ELIB - SuUB Bremen
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