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Original article
Mutation-specific Fabry disease patient-derived cell model to evaluate the amenability to chaperone therapy

Authors

  1. Correspondence to Dr Malte Lenders, Internal Medicine D, Department of Nephrology, Hypertension and Rheumatology, University Hospital Muenster, Muenster D-48149, Germany; malte.lenders{at}ukmuenster.de
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Citation

Lenders M, Stappers F, Niemietz C, et al
Mutation-specific Fabry disease patient-derived cell model to evaluate the amenability to chaperone therapy

Publication history

  • Received January 8, 2019
  • Revised March 14, 2019
  • Accepted March 19, 2019
  • First published April 22, 2019.
Online issue publication 
July 26, 2019

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