Comparing the alpha-galactosidase A biochemical properties from healthy individuals and Fabry disease patients-Reference-Cited by-同舟云学术

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Comparing the alpha-galactosidase A biochemical properties from healthy individuals and Fabry disease patients

Published:2015-05 Issue: Volume:445 Page:60-64
ISSN:0009-8981
Container-title:Clinica Chimica Acta
language:en
Short-container-title:Clinica Chimica Acta

Author:

Daitx Vanessa Vitcoski,Mezzalira Jamila,Moraes Vitória da Costa,Breier Ana Carolina,Cé Jaqueline,Coelho Janice Carneiro

Funder

CNPq

FAPERGS

Publisher

Elsevier BV

Subject

Biochemistry (medical),Clinical Biochemistry,Biochemistry,General Medicine

Reference33 articles.

1. Alpha-galactosidase A deficiency: Fabry disease;Desnick,2001

2. Prevalence of lysosomal storage disorders;Meikle;JAMA,1999

3. High incidence of later-onset Fabry disease revealed by newborn screening;Spada;Am J Hum Genet,2006

4. Newborn screening for Fabry disease in Taiwan reveals a high incidence of the later-onset GLA mutation c.936+919G>A (IVS4+919G>A);Hwu;Hum Mutat,2009

5. Newborn screening for lysosomal storage disorders in Hungary;Wittmann;JIMD Rep,2012

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Effects of fishmeal substitution by α-galactosidase hydrolytic soybean meal (EhSBM) on growth, antioxidant capacity, inflammatory responses and intestinal health of turbot juveniles (Scophthalmus maximus L.);Aquaculture;2023-01

2. Strong increase of leukocyte apha‐galactosidase A activity in two male patients with Fabry disease following oral chaperone therapy;Molecular Genetics & Genomic Medicine;2019-08-08

3. α-Galactosidases;Current Developments in Biotechnology and Bioengineering;2017

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