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POLG2
Supplementary Materials: Evaluation of Cytotoxicity and Α-Glucosidase Inhibitory Activity of Amide and Polyamino-Derivatives of Lupane Triterpenoids
Progressive External Ophthalmoplegia and Vision and Hearing Loss in a Patient with Mutations in POLG2 and OPA1
Gout Et Al Ultra-Mutation Targets Germline Alleles in an Infant Leukemia Recapitulation of Human Germline Coding Variation in An
WO 2016/115632 Al 28 July 2016 (28.07.2016) W P O P C T
Mitochondrial DNA Mutations Cause Various Diseases
Progressive External Ophthalmoplegia
See a Sample Report
Overview of Research on Fusion Genes in Prostate Cancer
Polymerase Gamma (POLG) Related Disorders Genetic Testing
Dominant Mutations in Mtdna Maintenance Gene SSBP1 Cause Optic Atrophy and Foveopathy
A Polymorphism of the POLG2 Gene Is Genetically Associated with the Invasiveness of Urinary Bladder Cancer in Japanese Males
Gnomad Lof Supplement
DNA Polymerase Gamma and Mitochondrial Disease: Understanding the Consequence of POLG Mutations
Mitochondrial Neurogastrointestinal Encephalopathy Due to Mutations in RRM2B
Progressive External Ophthalmoplegia and Vision and Hearing Loss in a Patient with Mutations in POLG2 and OPA1
Fifteen New Risk Loci for Coronary Artery Disease Highlight Arterial-Wall-Specific Mechanisms
Evaluation of Children with Suspected Mitochondrial Liver Disease
Human Mitochondrial DNA Replication Machinery and Disease. Matthew J Ouny G Southern Illinois University School of Medicine
Top View
Anterograde Regulation of Mitochondrial Genes and FGF21 Signaling by Hepatic LSD1
Screening of Polymerase Gamma 1 Gene with DHPLC, SURVEYOR Nuclease Strategy—ACMG 2007—Transgenomic
Reversal of Mitochondrial Defects with CSB-Dependent Serine Protease Inhibitors in Patient Cells of the Progeroid Cockayne Syndr
Blueprint Genetics Mitochondrial DNA Depletion Syndrome Panel
Mitochondrial/Metabolic Oligonucleotide Array CGH Analysis
Characterization of the Human Homozygous R182W POLG2 Mutation in Mitochondrial DNA Depletion Syndrome
POLG-Related Disorders and Their Neurological Manifestations
Blueprint Genetics POLG2 Single Gene Test
Association of Genetic Polymorphisms with Hepatitis C Virus-Related Liver Cirrhosis in Japan
POLG2 Antibody (C-Term) Purified Rabbit Polyclonal Antibody (Pab) Catalog # Ap2838b
POLG2 Deficiency Causes Adult-Onset Syndromic Sensory Neuropathy
De Novo Development of Mtdna Deletion Due to Decreased POLG and SSBP1 Expression in Humans
Transcriptome-Wide Analyses Indicate Mitochondrial Responses to Particulate Air Pollution Exposure
1 Fifteen New Risk Loci for Coronary Artery Disease Highlight Arterial Wall-Specific Mechanisms 1 Joanna M.M. Howson1, Wei Zhao2
AJHG MS 43461 Revised V3
Mitochondrial DNA Mutagenesis and Human Health Impacts
Camptocormia As a Novel Phenotype in a Heterozygous POLG2 Mutation