Case Report Identification of SLC22A5 Gene Mutation in a Family with Carnitine Uptake Defect
Schematic representation of the molecular mechanism by which estrogen... | Download Scientific Diagram
SLC22A5 Gene - GeneCards | OCTN2 Protein | OCTN2 Antibody
SLC22A5 - an overview | ScienceDirect Topics
SLC22A5 Membrane Protein Introduction - Creative Biolabs
Frontiers | A report of a pedigree with compound heterozygous mutations in the SLC22A5 gene
Graphic presentation of mutations/unclassified missense variant... | Download Scientific Diagram
SLC22A5 - Wikipedia
SLC22A5 Gene - GeneCards | OCTN2 Protein | OCTN2 Antibody
Glioma cells survival depends both on fatty acid oxidation and on functional carnitine transport by SLC22A5 - Juraszek - 2021 - Journal of Neurochemistry - Wiley Online Library
Molecules | Free Full-Text | SLC22A5 (OCTN2) Carnitine Transporter—Indispensable for Cell Metabolism, a Jekyll and Hyde of Human Cancer
Frontiers | Biochemical, Molecular, and Clinical Characterization of Patients With Primary Carnitine Deficiency via Large-Scale Newborn Screening in Xuzhou Area
SLC22A5 Gene - GeneCards | OCTN2 Protein | OCTN2 Antibody
SLC22A5 Gene - GeneCards | OCTN2 Protein | OCTN2 Antibody
Phenotype and genotype variation in primary carnitine deficiency | Genetics in Medicine
Molecules | Free Full-Text | SLC22A5 (OCTN2) Carnitine Transporter—Indispensable for Cell Metabolism, a Jekyll and Hyde of Human Cancer
Molecules | Free Full-Text | SLC22A5 (OCTN2) Carnitine Transporter—Indispensable for Cell Metabolism, a Jekyll and Hyde of Human Cancer
![PDF] SLC22A5 mutations in a patient with systemic primary carnitine deficiency: the first Korean case confirmed by biochemical and molecular investigation. | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/909337edf495a2114b24c3ca2e1929795e1cae59/3-Figure1-1.png "PDF] SLC22A5 mutations in a patient with systemic primary carnitine deficiency: the first Korean case confirmed by biochemical and molecular investigation. | Semantic Scholar")
PDF] SLC22A5 mutations in a patient with systemic primary carnitine deficiency: the first Korean case confirmed by biochemical and molecular investigation. | Semantic Scholar
SLC22A5 - an overview | ScienceDirect Topics
DNA sequencing of exon 1 from the SLC22A5 gene (A) demonstrating the... | Download Scientific Diagram
What is SLC22A5 Gene Carnitine deficiency NGS Genetic DNA Test ?
Functional Genetic Diversity in the High-Affinity Carnitine Transporter OCTN2 (SLC22A5) | Molecular Pharmacology
