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

Xiaomin Hou1, Nina Hagemann, Stefan Schoebel

  • 1Department of Physical Biochemistry, Max-Planck-Institute of Molecular Physiology, Dortmund, Germany.

The EMBO Journal
|March 8, 2011
PubMed

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