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

Please use this identifier to cite or link to this item: https://doi.org/10.1021/bi902057a

DC Field	Value
dc.title	Elimination of the native structure and solubility of the hVAPB MSP domain by the Pro56Ser mutation that causes amyotrophic lateral sclerosis
dc.contributor.author	Shi, J.
dc.contributor.author	Lua, S.
dc.contributor.author	Tong, J.S.
dc.contributor.author	Song, J.
dc.date.accessioned	2011-11-29T06:09:59Z
dc.date.available	2011-11-29T06:09:59Z
dc.date.issued	2010
dc.identifier.citation	Shi, J., Lua, S., Tong, J.S., Song, J. (2010). Elimination of the native structure and solubility of the hVAPB MSP domain by the Pro56Ser mutation that causes amyotrophic lateral sclerosis. Biochemistry 49 (18) : 3887-3897. ScholarBank@NUS Repository. https://doi.org/10.1021/bi902057a
dc.identifier.issn	00062960
dc.identifier.issn	15204995
dc.identifier.uri	http://scholarbank.nus.edu.sg/handle/10635/28830
dc.description.uri	http://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1021/bi902057a
dc.source	Scopus
dc.type	Article
dc.contributor.department	BIOCHEMISTRY
dc.contributor.department	BIOLOGICAL SCIENCES
dc.description.doi	10.1021/bi902057a
dc.description.sourcetitle	Biochemistry
dc.description.volume	49
dc.description.issue	18
dc.description.page	3887-3897
dc.description.coden	BICHA
dc.identifier.isiut	000277212400012
Appears in Collections:	Staff Publications

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