Mutation identification of Fabry disease in families with other lysosomal storage disorders-Reference-Cited by-同舟云学术

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Mutation identification of Fabry disease in families with other lysosomal storage disorders

Published:2012-12-28 Issue:3 Volume:84 Page:281-285
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clin Genet

Author:

Zampetti A,Fania L,Antuzzi D¹,Giurdanella F,Gnarra M,Bertola F²,Lualdi S³,Filocamo M³,Morrone A,Feliciani C

Affiliation:

1. Department of Pediatric Sciences; Policlinico “A. Gemelli”, Università Cattolica del Sacro Cuore; Rome; Italy

2. Consortium for Human Molecular Genetics; University of Milano-Bicocca; Monza; Italy

3. Centro di Diagnostica Genetica e Biochimica delle Malattie Metaboliche; Istituto G. Gaslini; Genova; Italy

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference23 articles.

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

2. Fabry disease;Germain;Orphanet J Rare Dis,2010

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

4. Fabry disease in children and the effects of enzyme replacement treatment;Pintos-Morell;Eur J Pediatr,2009

Cited by 1 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. New Advanced Strategies for the Treatment of Lysosomal Diseases Affecting the Central Nervous System;Current Pharmaceutical Design;2019-09-04

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