Detection of 8 new mutations in the α-galactosidase A gene in Fabry disease-Reference-Cited by-同舟云学术

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Detection of 8 new mutations in the α-galactosidase A gene in Fabry disease

Published:1994 Issue:4 Volume:3 Page:667-669
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Hum Mol Genet

Author:

Davies Joanna,Christomanou Helen,Winchester Bryan,Malcolm Susan

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/3/4/667/2642003/3-4-667.pdf

Cited by 27 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. High incidence of co-existing factors significantly modifying the phenotype in patients with Fabry disease;Gene;2019-03

2. Risk factors for severe clinical events in male and female patients with Fabry disease treated with agalsidase beta enzyme replacement therapy: Data from the Fabry Registry;Molecular Genetics and Metabolism;2016-09

3. Fabry disease in patients with hypertrophic cardiomyopathy: a practical approach to diagnosis;Journal of Human Genetics;2016-05-26

4. Time to treatment benefit for adult patients with Fabry disease receiving agalsidase β: data from the Fabry Registry;Journal of Medical Genetics;2016-03-18

5. Fabry disease: A new approach for the screening of females in high-risk groups;Clinical Biochemistry;2014-05

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