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- Peroksisomale Sykdommer V01
- Gnomad Lof Supplement
- Identification of a Novel Mutation in PEX10 in a Patient with Attenuated
- PEX12 Interacts with PEX5 and PEX10 and Acts Downstream of Receptor Docking in Peroxisomal Matrix Protein Import Chia-Che Chang, Daniel S
- Blueprint Genetics Peroxisomal Disorders Panel
- Requirement of the C3HC4 Zinc RING Finger of the Arabidopsis PEX10 for Photorespiration and Leaf Peroxisome Contact with Chloroplasts
- Liver Diseases Genetic Testing Program
- Peroxisome Quality Control and Dysregulated Lipid Metabolism in Neurodegenerative Diseases Doo Sin Jo1,Nayeonpark2 and Dong-Hyung Cho1,2
- Functional Characterization of the Human Peroxins PEX3 and PEX19, Proteins Essential for Early Peroxisomal Membrane Biogenesis
- Identification of PEX10, the Gene Defective in Complementation
- Targeted Genes and Methodology Details for Inborn Errors of Metabolism Custom Gene Panel
- Genetic and Molecular Bases of Peroxisome Biogenesis Disorders
- Next Generation Sequencing (NGS)
- Genomic Unity® Prenatal Analysis
- Identification of Novel Mutations in PEX2, PEX6, PEX10, PEX12 And
- Peroxisome Biogenesis Disorders in the Zellweger Spectrum: an Overview of Current Diagnosis, Clinical Manifestations, and Treatment Guidelines
- Diagnostic Genetic Testing Requisition
- SSIEM Academy
- Requirement of the C3HC4 Zinc RING Finger of the Arabidopsis PEX10 for Photorespiration and Leaf Peroxisome Contact with Chloroplasts
- Multi-Level Proteomics Reveals Host-Perturbation Strategies Of
- EGL Test Description
- Ataxia with Novel Compound Heterozygous PEX10 Mutations and a Literature Review of PEX10-Related Peroxisome Biogenesis Disorders T
- Different Functions of the C3HC4 Zinc RING Finger Peroxins PEX10, PEX2
- Zellweger Spectrum Disorders
- A Novel Missense Variant in ACAA1 Contributes to Early-Onset
- Athpex10, a Nuclear Gene Essential for Peroxisome and Storage Organelle Formation During Arabidopsis Embryogenesis
- Anaerobic Peroxisomes in Mastigamoeba Balamuthi
- Compartmentalization of the Plant Peroxin, Atpex10p, Within Subdomain(S) of ER$
- Novel Mutations in the PEX12 Gene of Patients with a Peroxisome Biogenesis Disorder
- Prevalence and Incidence of Rare Diseases: Bibliographic Data
- ᵪ ᵪ Patient / Legal Guardian (Date, Signature) Doctor (Date, Signature)
- Prevalence and Incidence of Rare Diseases
- The First Patient with a Pure 1P36 Microtriplication Associated With
- Genomic Unity® Neurology Analysis
- Zellweger Syndrome Spectrum
- Identification and Characterization of Three Peroxins—PEX6, PEX10 and PEX12—Involved in Glycosome Biogenesis in Trypanosoma Bruceii
- Novel Mutations in the PEX2 Gene of Four Unrelated Patients with a Peroxisome Biogenesis Disorder