SLC22A5 Gene - GeneCards | OCTN2 Protein | OCTN2 Antibody
Case Report Identification of SLC22A5 Gene Mutation in a Family with Carnitine Uptake Defect
Phenotype and genotype variation in primary carnitine deficiency | Genetics in Medicine
![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
A) The primary function of the plasma membrane carnitine transporter.... | Download Scientific Diagram
SLC22A5 - an overview | ScienceDirect Topics
SLC22A5 Gene - GeneCards | OCTN2 Protein | OCTN2 Antibody
Graphic presentation of mutations/unclassified missense variant... | Download Scientific Diagram
![PDF] Identification of SLC22A5 Gene Mutation in a Family with Carnitine Uptake Defect | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/f809e8360ccae2c9351b4387e3de330e41978c2d/4-Table2-1.png "PDF] Identification of SLC22A5 Gene Mutation in a Family with Carnitine Uptake Defect | Semantic Scholar")
PDF] Identification of SLC22A5 Gene Mutation in a Family with Carnitine Uptake Defect | Semantic Scholar
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
allele, haplotype and diplotype frequencies of the SLC22A4 and SLC22A5 gene variants in New Zealand Crohn's disease (CD) patients and control subjects
SLC22A5 - Wikipedia
SLC22A5 Membrane Protein Introduction - Creative Biolabs
SLC22A5 - an overview | ScienceDirect Topics
What is SLC22A5 Gene Carnitine deficiency NGS Genetic DNA Test ?
SLC22A5 Gene - GeneCards | OCTN2 Protein | OCTN2 Antibody
Pharmacological and pathophysiological roles of carnitine/organic cation transporters (OCTNs: SLC22A4, SLC22A5 and Slc22a21) - Tamai - 2013 - Biopharmaceutics & Drug Disposition - Wiley Online Library
Tight junction protein ZO-1 controls organic cation/carnitine transporter OCTN2 (SLC22A5) in a protein kinase C-dependent way - ScienceDirect
Schematic representation of the molecular mechanism by which estrogen... | Download Scientific Diagram
DNA sequencing of exon 1 from the SLC22A5 gene (A) demonstrating the... | Download Scientific Diagram
SLC22A5 Gene - GeneCards | OCTN2 Protein | OCTN2 Antibody
Maternal systemic primary carnitine deficiency uncovered by newborn screening: Clinical, biochemical, and molecular aspects | Genetics in Medicine
SLC22A5 Gene - GeneCards | OCTN2 Protein | OCTN2 Antibody
Carnitine transport and fatty acid oxidation - ScienceDirect
Maternal Primary Carnitine Deficiency and a Novel Solute Carrier Family 22 Member 5 (SLC22A5) Mutation
Frontiers | Newborn Screening and Genetic Analysis Identify Six Novel Genetic Variants for Primary Carnitine Deficiency in Ningbo Area, China
