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

Item

ITEM ACTIONSEXPORT

Add to Basket

Local TagsRelease HistoryDetailsSummary

Released

Journal Article

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

MPS-Authors

Hou, Xiaomin
Max Planck Institute of Molecular Physiology, Max Planck Society;

Schoebel, Stefan
Max Planck Institute of Molecular Physiology, Max Planck Society;

/persons/resource/persons98681

Blankenfeldt, Wulf
Abt. III: Physikalische Biochemie, Max Planck Institute of Molecular Physiology, Max Planck Society;

/persons/resource/persons98693

Goody, Roger S.
Abt. III: Physikalische Biochemie, Max Planck Institute of Molecular Physiology, Max Planck Society;

/persons/resource/persons98700

Itzen, Aymelt
Abt. III: Physikalische Biochemie, Max Planck Institute of Molecular Physiology, Max Planck Society;

External Resource

No external resources are shared

Fulltext (restricted access)

There are currently no full texts shared for your IP range.

Fulltext (public)

There are no public fulltexts stored in PuRe

Supplementary Material (public)

There is no public supplementary material available

Citation

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.

Cite as: https://hdl.handle.net/11858/00-001M-0000-0014-00F0-F

Abstract

There is no abstract available