NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 9, mitochon - Protein

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NDUFA9 point mutations cause a variable mitochondrial complex I assembly defect. [Clin Genet. 2018]
NDUFA9 point mutations cause a variable mitochondrial complex I assembly defect.
Baertling F, Sánchez-Caballero L, van den Brand MAM, Fung CW, Chan SH, Wong VC, Hellebrekers DME, de Coo IFM, Smeitink JAM, Rodenburg RJT, et al. Clin Genet. 2018 Jan; 93(1):111-118. Epub 2017 Nov 21.
Gene knockout using transcription activator-like effector nucleases (TALENs) reveals that human NDUFA9 protein is essential for stabilizing the junction between membrane and matrix arms of complex I. [J Biol Chem. 2013]
Gene knockout using transcription activator-like effector nucleases (TALENs) reveals that human NDUFA9 protein is essential for stabilizing the junction between membrane and matrix arms of complex I.
Stroud DA, Formosa LE, Wijeyeratne XW, Nguyen TN, Ryan MT. J Biol Chem. 2013 Jan 18; 288(3):1685-90. Epub 2012 Dec 5.
Defective NDUFA9 as a novel cause of neonatally fatal complex I disease. [J Med Genet. 2012]
Defective NDUFA9 as a novel cause of neonatally fatal complex I disease.
van den Bosch BJ, Gerards M, Sluiter W, Stegmann AP, Jongen EL, Hellebrekers DM, Oegema R, Lambrichs EH, Prokisch H, Danhauser K, et al. J Med Genet. 2012 Jan; 49(1):10-5. Epub 2011 Nov 23.

RefSeq genomic sequence
See the genomic reference sequence for the NDUFA9 gene (NG_032124.1).
RefSeq mRNA
See reference mRNA sequence for the NDUFA9 gene (NM_005002.5).

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MODBASE, Database of Comparative Protein Structure Models (Sali Lab/UCSF) [MODBASE, Database of Comparat...]
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Transcript/Protein Information [PANTHER Classification System]
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Find Quality Antibodies [GeneTex Inc]
Find Quality Antibodies
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