SLC22A5 Gene - GeneCards | OCTN2 Protein | OCTN2 Antibody
Phenotype and genotype variation in primary carnitine deficiency | Genetics in Medicine
SLC22A5 gene
What is SLC22A5 Gene Carnitine deficiency NGS Genetic DNA Test ?
IJMS | Free Full-Text | PGC-1α and MEF2 Regulate the Transcription of the Carnitine Transporter OCTN2 Gene in C2C12 Cells and in Mouse Skeletal Muscle
SLC22A5 - an overview | ScienceDirect Topics
Maternal systemic primary carnitine deficiency uncovered by newborn screening: Clinical, biochemical, and molecular aspects | Genetics in Medicine
Carnitine Deficiency, Systemic Primary - The Medical Biochemistry Page
L -Carnitine and its carrier SLC22A5 mediated sensing and signaling | Download Scientific Diagram
A) The primary function of the plasma membrane carnitine transporter.... | 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]
SLC22A5 - an overview | ScienceDirect Topics
Maternal Primary Carnitine Deficiency and a Novel Solute Carrier Family 22 Member 5 (SLC22A5) Mutation - Michael Jakoby, Amruta Jaju, Aundrea Marsh, Andrew Wilber, 2021
![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
Pharmacological and pathophysiological roles of carnitine/organic cation transporters (OCTNs: SLC22A4, SLC22A5 and Slc22a21) - Tamai - 2013 - Biopharmaceutics & Drug Disposition - Wiley Online Library
SLC22A5 gene | Semantic Scholar
Phenotype and genotype variation in primary carnitine deficiency - Genetics in Medicine
Carnitine transport and fatty acid oxidation. - Abstract - Europe PMC
DNA sequencing of exon 1 from the SLC22A5 gene (A) demonstrating the... | Download Scientific Diagram
Molecules | Free Full-Text | SLC22A5 (OCTN2) Carnitine Transporter—Indispensable for Cell Metabolism, a Jekyll and Hyde of Human Cancer
Primary carnitine deficiency in two sisters with intractable epilepsy and reversible metabolic cardiomyopathy: Two case reports
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
Functional Genetic Diversity in the High-Affinity Carnitine Transporter OCTN2 (SLC22A5) | Molecular Pharmacology
Frontiers | Newborn Screening and Genetic Analysis Identify Six Novel Genetic Variants for Primary Carnitine Deficiency in Ningbo Area, China
Case Report Identification of SLC22A5 Gene Mutation in a Family with Carnitine Uptake Defect
