NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 8, mitochond - Protein

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NDUFB8 Mutations Cause Mitochondrial Complex I Deficiency in Individuals with Leigh-like Encephalomyopathy. [Am J Hum Genet. 2018]
NDUFB8 Mutations Cause Mitochondrial Complex I Deficiency in Individuals with Leigh-like Encephalomyopathy.
Piekutowska-Abramczuk D, Assouline Z, Mataković L, Feichtinger RG, Koňařiková E, Jurkiewicz E, Stawiński P, Gusic M, Koller A, Pollak A, et al. Am J Hum Genet. 2018 Mar 1; 102(3):460-467. Epub 2018 Feb 8.
Identification of 167 polymorphisms in 88 genes from candidate neurodegeneration pathways. [Gene. 1999]
Identification of 167 polymorphisms in 88 genes from candidate neurodegeneration pathways.
Emahazion T, Jobs M, Howell WM, Siegfried M, Wyöni PI, Prince JA, Brookes AJ. Gene. 1999 Oct 1; 238(2):315-24.
Using a quantitative quadruple immunofluorescent assay to diagnose isolated mitochondrial Complex I deficiency. [Sci Rep. 2017]
Using a quantitative quadruple immunofluorescent assay to diagnose isolated mitochondrial Complex I deficiency.
Ahmed ST, Alston CL, Hopton S, He L, Hargreaves IP, Falkous G, Oláhová M, McFarland R, Turnbull DM, Rocha MC, et al. Sci Rep. 2017 Nov 15; 7(1):15676. Epub 2017 Nov 15.

RefSeq protein isoforms
See 3 reference sequence protein isoforms for the NDUFB8 gene.

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NP_001271297 [Domain Mapping of Disease Mut...]
NP_001271297
Domain Mapping of Disease Mutations
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Protein