A structural basis for Lowe syndrome caused by mutations in the Rab-binding 
domain of OCRL1

Hou, Xiaomin; Hagemann, Nina; Schoebel, Stefan; Blankenfeldt, Wulf; Goody, Roger S.; Erdmann, Kai S.; Itzen, Aymelt

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A structural basis for Lowe syndrome caused by mutations in the Rab-binding domain of OCRL1

Hou, X., Hagemann, N., Schoebel, S., Blankenfeldt, W., Goody, R. S., Erdmann, K. S., et al. (2011). A structural basis for Lowe syndrome caused by mutations in the Rab-binding domain of OCRL1. The EMBO Journal, 30(8): 1, pp. 1659-1670. Retrieved from http://dx.doi.org/10.1038/emboj.2011.60.

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Item Permalink: https://hdl.handle.net/11858/00-001M-0000-0014-00F0-F Version Permalink: https://hdl.handle.net/11858/00-001M-0000-0014-00F1-D

Genre: Journal Article

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Creators:
Hou, Xiaomin¹, Author
Hagemann, Nina, Author
Schoebel, Stefan¹, Author
Blankenfeldt, Wulf², Author
Goody, Roger S.², Author
Erdmann, Kai S., Author
Itzen, Aymelt², Author

Affiliations:
1Max Planck Institute of Molecular Physiology, Max Planck Society, ou_1753286
2Abt. III: Physikalische Biochemie, Max Planck Institute of Molecular Physiology, Max Planck Society, ou_1753289

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Free keywords: Dent disease; Lowe syndrome; OCRL; Rab; Rab8

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Language(s): eng - English

Dates: Date issued: 2011

Publication Status: Issued

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Rev. Type: Peer

Identifiers: eDoc: 563765
URI: http://dx.doi.org/10.1038/emboj.2011.60

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Title: The EMBO Journal

Source Genre: Journal

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Pages: - Volume / Issue: 30 (8) Sequence Number: 1 Start / End Page: 1659 - 1670 Identifier: -