Biochemical and metabolic genetics

123 - The First Case of FLAD1 Associated Multiple Acyl-CoA Dehydrogenace Deficiency Identified by Newborn Screening

Previous Eposter
117 - Late-Onset Glutaric Acidemia Type 2 Is Associated with Increased Superoxide Levels and Decreased ATP Production, Spare Respiratory Capacity, and Levels of ETFDH Functional Partners

Next Eposters
124 - Diagnostic Yield of Neuronal Ceroid Lipofuscinoses Molecular Genetic Tests: Phenotype and Genotype of Neuronal Ceroid Lipofuscinoses
126 - A Case of Infantile Onset Pompe Disease Presenting with Non-Immune Hydrops Fetalis
132 - Inflammation-Associated Cytokines and Wnt Gene Expression in the Intestinal Stem Cell Niche
133 - Identifying Rare Metabolic Disorders of Energy Dysfunction in Patients with Treatment-Resistant Depression
136 - Biochemical Diagnosis of Mannosyl-Oligosaccharide Glucosidase Type of Congenital Disorders of Glycosylation (MOGS-CDG)
137 - Variable Expressivity of a Variant in the OTC Promoter Region Causing Hyperammonemia Across Generations
141 - Leigh Syndrome In An Adolescent With a Rare Mutation of PDHA1
143 - Dizygotic Twins Presenting with Hypertyrosinemia and Discordant Succinylacetone Results
149 - Creatine Metabolism in Patients with Urea Cycle Disorders
153 - Differences in Phenylalanine Levels and White Matter Changes in Three Siblings with Phenylketonuria