Ten-year outcome of enzyme replacement therapy with agalsidase beta in patients with Fabry disease-Reference-Cited by-同舟云学术

Ten-year outcome of enzyme replacement therapy with agalsidase beta in patients with Fabry disease

Published:2015-03-20 Issue:5 Volume:52 Page:353-358
ISSN:0022-2593
Container-title:Journal of Medical Genetics
language:en
Short-container-title:J Med Genet

Author:

Germain Dominique P,Charrow Joel,Desnick Robert J,Guffon Nathalie,Kempf Judy,Lachmann Robin H,Lemay Roberta,Linthorst Gabor E,Packman Seymour,Scott C Ronald,Waldek Stephen,Warnock David G,Weinreb Neal J,Wilcox William R

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference27 articles.

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4. Angiokeratoma corporis diffusum—Fabry's disease;Colombi;Helv Med Acta,1967

5. Anderson-Fabry disease: clinical manifestations and impact of disease in a cohort of 98 hemizygous males;MacDermot;J Med Genet,2001

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