Literature DB >> 18645174

Corticobasal syndrome and primary progressive aphasia as manifestations of lrrk2 gene mutations.

Owen A Ross, Mathias Toft, Kristoffer Haugarvoll.   

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Year:  2008        PMID: 18645174     DOI: 10.1212/01.wnl.0000320511.30222.dd

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


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  1 in total

1.  Leucine-rich repeat kinase 2 gene-associated disease: redefining genotype-phenotype correlation.

Authors:  Christian Wider; Dennis W Dickson; Zbigniew K Wszolek
Journal:  Neurodegener Dis       Date:  2010-03-03       Impact factor: 2.977

  1 in total

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