A convenient approach to facilitate monitoring Gaucher disease progression and therapeutic response

A convenient approach to facilitate monitoring Gaucher disease progression and therapeutic response

© 2017 The Royal Society of Chemistry. Gaucher disease (GD) is caused by mutations on the GBA1 gene leading to deficiency in acid β-glucosidase (GCase) and subsequent accumulation of its substrates, glucosylceramide (GlcC) and glucosylsphingosine (GlcS). GlcS in plasma has been proposed as a highly...

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Bibliographic Details
Main Authors: Wujuan Zhang, Melissa Oehrle, Carlos E. Prada, Ida Vanessa D. Schwartz, Somchai Chutipongtanate, Duangrurdee Wattanasirichaigoon, Venette Inskeep, Mei Dai, Dao Pan, Ying Sun, Kenneth D.R. Setchell
Other Authors: Cincinnati Children's Hospital Medical Center
Format: Article
Published: 2018
Subjects:
Biochemistry, Genetics and Molecular Biology
Chemistry
Environmental Science
Online Access:https://repository.li.mahidol.ac.th/handle/123456789/41803
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Institution: Mahidol University

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https://repository.li.mahidol.ac.th/handle/123456789/41803

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