NADH dehydrogenase subunit 4L (mitochondrion) [Homo sapiens]

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A novel PCLN-1 gene mutation in familial hypomagnesemia with hypercalciuria and atypical phenotype. [Pediatr Nephrol. 2007]
A novel PCLN-1 gene mutation in familial hypomagnesemia with hypercalciuria and atypical phenotype.
Sanjad SA, Hariri A, Habbal ZM, Lifton RP. Pediatr Nephrol. 2007 Apr; 22(4):503-8. Epub 2006 Nov 23.
The role of mtDNA background in disease expression: a new primary LHON mutation associated with Western Eurasian haplogroup J. [Hum Genet. 2002]
The role of mtDNA background in disease expression: a new primary LHON mutation associated with Western Eurasian haplogroup J.
Brown MD, Starikovskaya E, Derbeneva O, Hosseini S, Allen JC, Mikhailovskaya IE, Sukernik RI, Wallace DC. Hum Genet. 2002 Feb; 110(2):130-8. Epub 2002 Jan 24.
Cryo-EM structures of complex I from mouse heart mitochondria in two biochemically defined states. [Nat Struct Mol Biol. 2018]
Cryo-EM structures of complex I from mouse heart mitochondria in two biochemically defined states.
Agip AA, Blaza JN, Bridges HR, Viscomi C, Rawson S, Muench SP, Hirst J. Nat Struct Mol Biol. 2018 Jul; 25(7):548-556. Epub 2018 Jun 18.

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YP_003024034 [Domain Mapping of Disease Mut...]
YP_003024034
Domain Mapping of Disease Mutations
Ensembl [Ensembl]
Ensembl
GlyGen glycoinformatics resource [GlyGen glycoinformatics resou...]
GlyGen glycoinformatics resource
Transcript/Protein Information [PANTHER Classification System]
Transcript/Protein Information
PANTHER Classification System
reagents [ExactAntigen/Labome]
reagents
ExactAntigen/Labome

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