Homo sapiens RAB39B, member RAS oncogene family (RAB39B), RefSeqGene o - Nucleotide

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Novel RAB39B Mutation Causes Parkinsonism in Males with Developmental Disorder. [Mov Disord Clin Pract. 2024]
Novel RAB39B Mutation Causes Parkinsonism in Males with Developmental Disorder.
Dayan R, Shkedi Rafid S, Baker Erdman H, Weill C, Shag A, Meiner V, Arkadir D. Mov Disord Clin Pract. 2024 Mar; 11(3):306-308. Epub 2024 Jan 31.
Deficiency of RAB39B Activates ER Stress-Induced Pro-apoptotic Pathway and Causes Mitochondrial Dysfunction and Oxidative Stress in Dopaminergic Neurons by Impairing Autophagy and Upregulating α-Synuclein. [Mol Neurobiol. 2023]
Deficiency of RAB39B Activates ER Stress-Induced Pro-apoptotic Pathway and Causes Mitochondrial Dysfunction and Oxidative Stress in Dopaminergic Neurons by Impairing Autophagy and Upregulating α-Synuclein.
Chiu CC, Weng YH, Yeh TH, Lu JC, Chen WS, Li AH, Chen YL, Wei KC, Wang HL. Mol Neurobiol. 2023 May; 60(5):2706-2728. Epub 2023 Jan 30.
Evolutionarily conserved regulators of tau identify targets for new therapies. [Neuron. 2023]
Evolutionarily conserved regulators of tau identify targets for new therapies.
Kim J, de Haro M, Al-Ramahi I, Garaicoechea LL, Jeong HH, Sonn JY, Tadros B, Liu Z, Botas J, Zoghbi HY. Neuron. 2023 Mar 15; 111(6):824-838.e7. Epub 2023 Jan 6.

Protein
Protein sequence from Nucleotide coding region
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Homo sapiens RAB39B, member RAS oncogene family (RAB39B), RefSeqGene on chromoso...
Homo sapiens RAB39B, member RAS oncogene family (RAB39B), RefSeqGene on chromosome X
gi|540344601|ref|NG_012626.2|

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Nucleotide