apolipoprotein A-I binding protein, isoform CRA_a, partial [Homo sapie - Protein

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Nuclear Mitochondrial Disorder Due to a Variant in NAXE in Two Unrelated Indian Children. [Indian J Pediatr. 2024]
Nuclear Mitochondrial Disorder Due to a Variant in NAXE in Two Unrelated Indian Children.
Rao SS, Bhavani GS, Jalan AB, Shenoy RD. Indian J Pediatr. 2024 Feb; 91(2):184-187. Epub 2023 Feb 11.
Identification of a novel homozygous mutation in NAXE gene associated with early-onset progressive encephalopathy by whole-exome sequencing: in silico protein structure characterization, molecular docking, and dynamic simulation. [Neurogenetics. 2022]
Identification of a novel homozygous mutation in NAXE gene associated with early-onset progressive encephalopathy by whole-exome sequencing: in silico protein structure characterization, molecular docking, and dynamic simulation.
Maalej M, Sfaihi L, Ammar M, Frikha F, Kharrat M, Alila-Fersi O, Mkaouar-Rebai E, Tlili A, Kammoun T, Fakhfakh F. Neurogenetics. 2022 Oct; 23(4):257-270. Epub 2022 Jul 11.
NAXE deficiency: A neurometabolic disorder of NAD(P)HX repair amenable for metabolic correction. [Mol Genet Metab. 2022]
NAXE deficiency: A neurometabolic disorder of NAD(P)HX repair amenable for metabolic correction.
Manor J, Calame D, Gijavanekar C, Fisher K, Hunter J, Mizerik E, Bacino C, Scaglia F, Elsea SH. Mol Genet Metab. 2022 Jun; 136(2):101-110. Epub 2022 Apr 18.

RefSeq genomic sequence
See the genomic reference sequence for the NAXE gene (NG_052542.1).
RefSeq protein
See the reference protein sequence for NAD(P)H-hydrate epimerase precursor (NP_658985.2).

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apolipoprotein A-I binding protein, isoform CRA_a, partial [Homo sapiens]
apolipoprotein A-I binding protein, isoform CRA_a, partial [Homo sapiens]
gi|119573326|gb|EAW52941.1||gnl|WGS |hCP1914711

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