Glioma cells survival depends both on fatty acid oxidation and on functional carnitine transport by SLC22A5 - Juraszek - 2021 - Journal of Neurochemistry - Wiley Online Library
Functional Genetic Diversity in the High-Affinity Carnitine Transporter OCTN2 (SLC22A5) | Molecular Pharmacology
Molecules | Free Full-Text | SLC22A5 (OCTN2) Carnitine Transporter—Indispensable for Cell Metabolism, a Jekyll and Hyde of Human Cancer
Phenotype and genotype variation in primary carnitine deficiency - ScienceDirect
SLC22A5 Gene - GeneCards | S22A5 Protein | S22A5 Antibody
anti-SLC22A5 antibody | anti-Human SLC22A5 Antibody-NP_001295051.1
Frontiers | Newborn Screening and Genetic Analysis Identify Six Novel Genetic Variants for Primary Carnitine Deficiency in Ningbo Area, China
Maternal systemic primary carnitine deficiency uncovered by newborn screening: Clinical, biochemical, and molecular aspects | Genetics in Medicine
![PDF] 20 Years After Discovery of the Causative Gene of Primary Carnitine Deficiency, How Much More Have We Known About the Disease? | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/651ba513a258b0a57dc15c728599dfc387fb11ea/3-Figure1-1.png "PDF] 20 Years After Discovery of the Causative Gene of Primary Carnitine Deficiency, How Much More Have We Known About the Disease? | Semantic Scholar")
PDF] 20 Years After Discovery of the Causative Gene of Primary Carnitine Deficiency, How Much More Have We Known About the Disease? | Semantic Scholar
proteins - How can carnitine enter the mitochondrial matrix without OCTN2? - Biology Stack Exchange
Genetic spectrum of pathogenic variants in the SLC22A5 gene. (A)... | Download Scientific Diagram
Anti-SLC22A5 Antibody (CAB1676) | WB, IF
Slc22a5 ORF Vector (Mouse) (pORF) | Applied Biological Materials Inc.
What is SLC22A5 Gene Carnitine deficiency NGS Genetic DNA Test ?
A novel pathogenic variant in the carnitine transporter gene, SLC22A5, in association with metabolic carnitine deficiency and cardiomyopathy features | BMC Cardiovascular Disorders | Full Text
SLC22A5 - Wikipedia
SLC22A5 - an overview | ScienceDirect Topics
SLC22A5 Membrane Protein Introduction - Creative Biolabs
Carnitine Deficiency, Systemic Primary - The Medical Biochemistry Page
L -Carnitine and its carrier SLC22A5 mediated sensing and signaling | Download Scientific Diagram
![Hong Kong Journal of Paediatrics [HK J Paediatr (New Series) 2013;18:167-173]](https://www.hkjpaed.org/figure/2013;18;167-173-fig1.jpg "Hong Kong Journal of Paediatrics [HK J Paediatr (New Series) 2013;18:167-173]")
Hong Kong Journal of Paediatrics [HK J Paediatr (New Series) 2013;18:167-173]
Frontiers | Biochemical, Molecular, and Clinical Characterization of Patients With Primary Carnitine Deficiency via Large-Scale Newborn Screening in Xuzhou Area
SLC22A5 gene | Semantic Scholar
Homepage of the SLC22A5 gene from our LOVD-China database for FAODs. | Download Scientific Diagram
