Varaico: Literature-Extracted Genetic Variants

Gene:GAA
Variant:p.S619R
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GAA

NM_000152.5:p.S619R

Associated Papers

Neutral sp2-iminosugars exploiting non-glycone interactions for selective acid α- and β-glucosidase activity modulation: Pharmacological chaperones for Gaucher and Pompe diseases.

García-Moreno MI et al.

European Journal of Medicinal Chemistry, 2026

Long-term observation of patients with advanced late-onset Pompe disease undergoing enzyme replacement therapy: A 15-year observation in a single center.

Mori-Yoshimura M et al.

Brain & Development, 2024

Biochemical and Genetic Testing of GAA in Over 30.000 Symptomatic Patients Suspected to Be Affected With Pompe Disease.

Balendran-Braun S et al.

Human Mutation, 2024

Diagnostic Yield of Chilaiditi's Sign in Advanced-Phase Late-Onset Pompe Disease.

Takahashi J et al.

Journal of Neuromuscular Diseases, 2022

Current status of newborn screening for Pompe disease in Japan.

Sawada T et al.

Orphanet Journal of Rare Diseases, 2021

Broad variation in phenotypes for common GAA genotypes in Pompe disease.

Niño MY et al.

Human Mutation, 2021

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.

Park KS

Children (basel, Switzerland), 2021

Newborn Screening for Pompe Disease.

Sawada T et al.

International Journal of Neonatal Screening, 2020

33073027 (PubMed )
Supplement: IJNS-06-00031-s001.zip › IJNS-711503-supplementary.xlsx › Table_S1

GAA variants and phenotypes among 1,079 patients with Pompe disease: Data from the Pompe Registry.

Reuser AJJ et al.

Human Mutation, 2019

31342611 (PubMed )
Supplement: HUMU-40-2146-s001.pdf

Newborn screening for Pompe disease in Japan: report and literature review of mutations in the GAA gene in Japanese and Asian patients.

Momosaki K et al.

Journal of Human Genetics, 2019

A computational method to characterize the missense mutations in the catalytic domain of GAA protein causing Pompe disease.

Thirumal Kumar D et al.

Journal of Cellular Biochemistry, 2019

A molecular analysis of the GAA gene and clinical spectrum in 38 patients with Pompe disease in Japan.

Fukuhara Y et al.

Molecular Genetics and Metabolism Reports, 2018

Enzyme therapy for hypertrophic cardiomyopathy in non-classical Pompe disease: Effectiveness of treatment.

Kim J et al.

Pediatrics International : Official Journal of the Japan Pediatric Society, 2017

[Pompe disease treatable by enzyme replacement therapy and the underlying autophagic dysfunction].

Fukuda T

No to Hattatsu = Brain and Development, 2015

Proteasome Inhibitor Bortezomib Enhances the Activity of Multiple Mutant Forms of Lysosomal α-Glucosidase in Pompe Disease.

Shimada Y et al.

Jimd Reports, 2015

Hypertrophic cardiomyopathy in pompe disease is not limited to the classic infantile-onset phenotype.

Lee DH et al.

Jimd Reports, 2014

Effects of enzyme replacement therapy on five patients with advanced late-onset glycogen storage disease type II: a 2-year follow-up study.

Furusawa Y et al.

Journal of Inherited Metabolic Disease, 2012

Close monitoring of initial enzyme replacement therapy in a patient with childhood-onset Pompe disease.

Ishigaki K et al.

Brain & Development, 2012

Biochemical and structural study on a S529V mutant acid α-glucosidase responsive to pharmacological chaperones.

Tajima Y et al.

Journal of Human Genetics, 2011

High-density areas on muscle CT in childhood-onset Pompe disease are caused by excess calcium accumulation.

Ishigaki K et al.

Acta Neuropathologica, 2010

The pharmacological chaperone 1-deoxynojirimycin increases the activity and lysosomal trafficking of multiple mutant forms of acid alpha-glucosidase.

Flanagan JJ et al.

Human Mutation, 2009

[Enzyme replacement therapy in a patient with Pompe disease].

Fujikawa Y et al.

No to Hattatsu = Brain and Development, 2007

Structural and biochemical studies on Pompe disease and a "pseudodeficiency of acid alpha-glucosidase".

Tajima Y et al.

Journal of Human Genetics, 2007

New GAA mutations in Japanese patients with GSDII (Pompe disease).

Pipo JR et al.

Pediatric Neurology, 2003

Efficacy of avalglucosidase alfa in infantile-onset Pompe disease with high anti-alglucosidase alfa antibody titers.

Park AY et al.

Pediatrics International : Official Journal of the Japan Pediatric Society, 0

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Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."