Tissue-specific X chromosome inactivation studies as a decision-making criteria for enzyme replacement therapy in female heterozygotes for Fabry disease
Author:
Publisher
Elsevier BV
Subject
Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism
Cited by 5 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. Modelling the neuropathology of lysosomal storage disorders through disease-specific human induced pluripotent stem cells;Experimental Cell Research;2019-07
2. Ten-year outcome of enzyme replacement therapy with agalsidase beta in patients with Fabry disease;Journal of Medical Genetics;2015-03-20
3. Adult patients with Fabry disease: what does the cardiologist need to know?: Table 1;Heart;2015-03-11
4. Clinical prodromes of neurodegeneration in Anderson-Fabry disease;Neurology;2015-03-11
5. Cerebrovascular Involvement in Fabry Disease;Stroke;2015-01
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