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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;

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

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

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

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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: http://hdl.handle.net/11858/00-001M-0000-0014-00F0-F
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