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spg20 protein, human
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SPG20 mutation in three siblings with familial hereditary spastic paraplegia.
Recurrent null mutation in SPG20 leads to Troyer syndrome.
Different expression levels of spartin cause broad spectrum of cellular consequences in human neurob…
Methylation changes of SIRT1, KLF4, DAPK1 and SPG20 in B-lymphocytes derived from follicular and dif…
Chromosome mis-segregation and cytokinesis failure in trisomic human cells.
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New Genes in the Carcinogenesis of Colorectal Cancer
Diagnostic Potential of Hypermethylated DNA in Colorectal Cancer
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