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PDSS1
Supplementary Materials: Evaluation of Cytotoxicity and Α-Glucosidase Inhibitory Activity of Amide and Polyamino-Derivatives of Lupane Triterpenoids
Metabolic Targets of Coenzyme Q10 in Mitochondria
Human Mitochondrial Pathologies of the Respiratory Chain and ATP Synthase: Contributions from Studies of Saccharomyces Cerevisiae
COQ2 Gene Coenzyme Q2, Polyprenyltransferase
Mitochondrial Diseases: Expanding the Diagnosis in the Era of Genetic Testing
SSIEM Classification of Inborn Errors of Metabolism 2011
Carrier Screening Panel
Mitochondrial Function and Lifespan of Mice with Controlled Ubiquinone Biosynthesis
Mutations in Ubiquinone Deficiency and Oxidative Phosphorylation Disorders
Combined Defects in Oxidative Phosphorylation and Fatty Acid Β-Oxidation in Mitochondrial Disease
Molecular Epidemiology of Mitochondrial Cardiomyopathy:A Search Among Mitochondrial and Nuclear Genes
Rescue of Primary Ubiquinone Deficiency Due to a Novel COQ7 Defect Using 2,4–Dihydroxybensoic Acid
Comprehensive Mitochondrial Nuclear Gene Panel
Interpretation of Genomic Sequencing Results in Healthy and Ill Newborns: Results from the Babyseq Project
Mitochondrial Diseases Beyond the Brain
Mitochondrial DNA (Mtdna) Test Requisition
NIH Public Access Author Manuscript Dev Disabil Res Rev
A Personalized Model of COQ2 Nephropathy Rescued by the Wild-Type COQ2 Allele Or Dietary Coenzyme Q10 Supplementation
Top View
Genes and Variants Underlying Human Congenital Lactic Acidosis—From Genetics to Personalized Treatment
Mutations in Coenzyme Q10 Biosynthetic Genes
Genepanel Mitochondrial Diseases Genepanel Paediatric Cardiomyopathy AARS2 AARS2 ABAT ABCC6 ACAD9 ABCC9 ACO2 ACAD8 AFG3L2 ACAD9
Fatal Neonatal Encephalopathy and Lactic Acidosis Caused by a Homozygous Loss-Of-Function Variant in COQ9
Neurometabolic Implications of Coenzyme Q10 Deficiency: Pathogenesis, Detection and Treatment 1
Prenyldiphosphate Synthase, Subunit 1 (PDSS1)
(Coq10) Deficiency
ATM Regulates ATP Levels Through NRF1)
Blueprint Genetics Comprehensive Metabolism Panel
Leigh Syndrome Nuclear Gene Panel
Mitochondrial/Metabolic Oligonucleotide Array CGH Analysis
Comprehensive Diagnosis for Mitochondrial Disorders
Treatable Genetic Diseases Are Enriched in the General Psychiatric Population
Physician's Guide to the Diagnosis, Treatment, and Follow-Up Of
Impact of Chemical Analogs of 4-Hydroxybenzoic Acid on Coenzyme Q Biosynthesis: from Inhibition to Bypass of Coenzyme Q Deficiency Fabien Pierrel
Coenzyme Q10 in the Treatment of Mitochondrial Disease
Panel Nmg4 Mitocondriales
Download Gene List