Varaico: Literature-Extracted Genetic Variants

Gene:GLA
Variant:p.S345*
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GLA

NM_000169.3:p.S345*

Associated Papers

Fabry Disease and the Effectiveness of Enzyme Replacement Therapy (ERT) in Left Ventricular Hypertrophy (LVH) Improvement: A Review and Meta-Analysis.

Lee CL et al.

International Journal of Medical Sciences, 2022

Genomic screening of Fabry disease in young stroke patients: the Taiwan experience and a review of the literature.

Lee TH et al.

European Journal of Neurology, 2019

30103270 (PubMed )
Supplement: ENE-26-553-s001.docx

Fabry disease in a Japanese population-molecular and biochemical characteristics.

Sakuraba H et al.

Molecular Genetics and Metabolism Reports, 2018

Improvement in the sensitivity of newborn screening for Fabry disease among females through the use of a high-throughput and cost-effective method, DNA mass spectrometry.

Lu YH et al.

Journal of Human Genetics, 2018

Nano-LC-MS/MS for Quantification of Lyso-Gb3 and Its Analogues Reveals a Useful Biomarker for Fabry Disease.

Sueoka H et al.

Plos One, 2015

High-throughput detection of common sequence variations of Fabry disease in Taiwan using DNA mass spectrometry.

Lee SH et al.

Molecular Genetics and Metabolism, 2014

Plasma globotriaosylsphingosine (lysoGb3) could be a biomarker for Fabry disease with a Chinese hotspot late-onset mutation (IVS4+919G>A).

Liao HC et al.

Clinica Chimica Acta; International Journal of Clinical Chemistry, 2013

Effects of enzyme replacement therapy for cardiac-type Fabry patients with a Chinese hotspot late-onset Fabry mutation (IVS4+919G>A).

Lin HY et al.

Bmj Open, 2013

Development of a highly sensitive immuno-PCR assay for the measurement of α-galactosidase A protein levels in serum and plasma.

Nakano S et al.

Plos One, 2013

Natural history of Fabry renal disease: influence of alpha-galactosidase A activity and genetic mutations on clinical course.

Branton MH et al.

Medicine, 2002

Identification of fifteen novel mutations and genotype-phenotype relationship in Fabry disease.

Altarescu GM et al.

Clinical Genetics, 2001

[Molecular genetics of Fabry disease].

Sakuraba H

Seikagaku. the Journal of Japanese Biochemical Society, 1989

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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."