Carrier frequency and predicted genetic prevalence of Pompe disease based on a general population database - ScienceDirect
Pompe Disease: Causes Types Symptoms Signs Diagnosis Treatment FAQs
Pompe Disease
CRISPR-mediated generation and characterization of a Gaa homozygous c.1935C>A (p.D645E) Pompe disease knock-in mouse model recapitulating human infantile onset-Pompe disease | Scientific Reports
Pompe disease causes, symptoms, diagnosis, prognosis & treatment
Pompe Disease - Symptoms, Causes, Treatment | NORD
Children | Free Full-Text | Two Approaches for a Genetic Analysis of Pompe Disease: A Literature Review of Patients with Pompe Disease and Analysis Based on Genomic Data from the General Population
Molecular Approaches for the Treatment of Pompe Disease | SpringerLink
GAA mutation spectrums in 27 Chinese late-onset Pompe patients. All... | Download Scientific Diagram
Biomolecules | Free Full-Text | Pompe Disease: New Developments in an Old Lysosomal Storage Disorder
Pompe disease symptoms | Pompe Disease News
Pompe disease inheritance | Pompe Disease News
Rescue of Advanced Pompe Disease in Mice with Hepatic Expression of Secretable Acid α-Glucosidase - ScienceDirect
Pompe Disease - Physiopedia
Enzyme Replacement Therapy Can Reverse Pathogenic Cascade in Pompe Disease - ScienceDirect
Pompe disease: MedlinePlus Genetics
Pompe's disease - The Lancet
Pompe Disease: a Clinical, Diagnostic, and Therapeutic Overview | Current Treatment Options in Neurology
Animals | Free Full-Text | Novel Mutation in the Feline GAA Gene in a Cat with Glycogen Storage Disease Type II (Pompe Disease)
Correction of oxidative stress enhances enzyme replacement therapy in Pompe disease | EMBO Molecular Medicine
Causes of Pompe Disease | Pompe Disease News
Types and frequency of GAA mutations in patients with Pompe disease. | Download Table
Frontiers | Induced pluripotent stem cell for modeling Pompe disease
