Elimination of the native structure and solubility of the hVAPB MSP domain by the Pro56Ser mutation that causes amyotrophic lateral sclerosis

10.1021/bi902057a

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Bibliographic Details
Main Authors: Shi, J., Lua, S., Tong, J.S., Song, J.
Other Authors: BIOCHEMISTRY
Format: Article
Published: 2011
Online Access:http://scholarbank.nus.edu.sg/handle/10635/28830
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Institution: National University of Singapore
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Summary:10.1021/bi902057a