ArticleThe EMBO journal2011
A structural basis for Lowe syndrome caused by mutations in the Rab-binding domain of OCRL1.
Xiaomin Hou et al.PubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.
54 papers cite it
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ArticleThe EMBO journal2011
Xiaomin Hou et al.PubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.