Phenotypical characterization of α-galactosidase A gene mutations identified in a large Fabry disease screening program in stroke in the young-Reference-Cited by-同舟云学术

Phenotypical characterization of α-galactosidase A gene mutations identified in a large Fabry disease screening program in stroke in the young

Published:2013-07 Issue:7 Volume:115 Page:1088-1093
ISSN:0303-8467
Container-title:Clinical Neurology and Neurosurgery
language:en
Short-container-title:Clinical Neurology and Neurosurgery

Author:

De Brabander Isabel,Yperzeele Laetitia,Ceuterick-De Groote Chantal,Brouns Raf,Baker Robert,Belachew Shibeshih,Delbecq Jean,De Keulenaer Gilles,Dethy Sophie,Eyskens François,Fumal Arnaud,Hemelsoet Dimitri,Hughes Derralynn,Jeangette Sandrine,Nuytten Dirk,Redondo Patricia,Sadzot Bernard,Sindic Christian,Sheorajpanday Rishi,Thijs Vincent,Van Broeckhoven Christine,De Deyn Peter P.

Funder

Shire, Belgium

Publisher

Elsevier BV

Subject

Neurology (clinical),General Medicine,Surgery

Reference28 articles.

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3. Plasma globotriaosylsphingosine as a biomarker of Fabry disease;Togawa;Molecular Genetics and Metabolism,2010

4. Belgian Fabry study: prevalence of Fabry disease in a cohort of 1000 young patients with cerebrovascular disease;Brouns;Stroke,2010

5. Prevalence of Fabry disease in female patients with late-onset hypertrophic cardiomyopathy;Chimenti;Circulation,2004

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