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In Vitro Enzyme Measurement to Test Pharmacological Chaperone Responsiveness in Fabry and Pompe Disease

The use of personalized medicine to treat rare monogenic diseases like lysosomal storage disorders (LSDs) is challenged by complex clinical trial designs, high costs, and low patient numbers. Hundreds of mutant alleles are implicated in most of the LSDs. The diseases are typically classified into 2...

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Bibliografske podrobnosti
izdano v:J Vis Exp
Main Authors: Lukas, Jan, Knospe, Anne-Marie, Seemann, Susanne, Citro, Valentina, Cubellis, Maria V., Rolfs, Arndt
Format: Artigo
Jezik:Inglês
Izdano: MyJove Corporation 2017
Teme:
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC5755676/
https://ncbi.nlm.nih.gov/pubmed/29286471
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3791/56550
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