Associated Papers
Whole-exome sequencing identifies mutations of KIF22 in spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type.
Min BJ et al.
American Journal of Human Genetics, 2011
Mechanism of ubiquitin recognition by the CUE domain of Vps9p.
Prag G et al.
Cell, 2003
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