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pubmed-article:16983677pubmed:abstractTextMutations in the Progranulin gene (PGRN) recently have been discovered to be associated with frontotemporal dementia (FTD) linked to 17q21 without identified MAPT mutations. The range of mutations of PGRN that can result in the FTD phenotype and the clinical presentation of patients with PGRN mutations have yet to be determined.lld:pubmed
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pubmed-article:16983677pubmed:articleTitleCharacteristics of frontotemporal dementia patients with a Progranulin mutation.lld:pubmed
pubmed-article:16983677pubmed:affiliationCognitive Neuroscience Section, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD 20892-1440, USA.lld:pubmed
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