Varaico: Literature-Extracted Genetic Variants

Gene:GLA
Variant:p.S276N
Back to variants list

GLA

NM_000169.3:p.S276N

Associated Papers

Redefining the Genetic Architecture of Hypertrophic Cardiomyopathy: Role of Intermediate-Effect Variants.

García Hernandez S et al.

Circulation, 2025

40879562 (PubMed )
Supplement: cir-152-1060-s002.xlsx › S2._HCM_cohort_variant_classif.

Lyso-Gb3 associates with adverse long-term outcome in patients with Fabry disease.

Nowak A et al.

Journal of Medical Genetics, 2022

33495303 (PubMed )
Supplement: jmedgenet-2020-107338supp001.pdf

Systematic cascade screening in the Danish Fabry Disease Centre: 20 years of a national single-centre experience.

Effraimidis G et al.

Plos One, 2022

Globotrioasylsphingosine Levels and Optical Coherence Tomography Angiography in Fabry Disease Patients.

Wiest MRJ et al.

Journal of Clinical Medicine, 2021

Fabry disease genotype, phenotype, and migalastat amenability: Insights from a national cohort.

Nowak A et al.

Journal of Inherited Metabolic Disease, 2020

Assessment of Gene Variant Amenability for Pharmacological Chaperone Therapy with 1-Deoxygalactonojirimycin in Fabry Disease.

Lukas J et al.

International Journal of Molecular Sciences, 2020

Pulmonary involvement in Fabry disease: effect of plasma globotriaosylsphingosine and time to initiation of enzyme replacement therapy.

Franzen D et al.

Bmj Open Respiratory Research, 2018

29713479 (PubMed )
Supplement: bmjresp-2018-000277supp001.pdf

The validation of pharmacogenetics for the identification of Fabry patients to be treated with migalastat.

Benjamin ER et al.

Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2017

27657681 (PubMed )
Supplement: gim2016122x1.zip › Supplemental_Appendix_2_12152015.xlsx › Unknown

Novel tools for extraction and validation of disease-related mutations applied to Fabry disease.

Kuipers R et al.

Human Mutation, 2010

20629180 (PubMed )
Supplement: supplement_1.pdf

Thirty-four novel mutations of the GLA gene in 121 patients with Fabry disease.

Schäfer E et al.

Human Mutation, 2005

Respiratory impairments in patients suffering from Fabry disease - A cross-sectional study.

Ahmed H et al.

Chronic Respiratory Disease, 0

38334083 (PubMed )
Supplement: sj-pdf-1-crd-10.1177_14799731231221821.pdf
Select a paper to view details
UCSC Genome Browser·Imprint·Privacy·Terms·Feedback·Email Updates·

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."