Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C-->T (Arg493X) mutation: an international initiative. (Q51971909)

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scientific article published in October 2007

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English	Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C-->T (Arg493X) mutation: an international initiative.	scientific article published in October 2007

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scholarly article

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Europe PubMed Central

19 April 2018

http://europepmc.org/abstract/MED/17826340

Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C-->T (Arg493X) mutation: an international initiative. (English)

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http://europepmc.org/abstract/MED/17826340

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haploinsufficiency

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Stuart Pickering-Brown

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Elisabeth McCarty Wood

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Dan H Geschwind

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Dan H Geschwind

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Gerard D Schellenberg

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Jennifer Gass

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Jennifer Adamson

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Salvatore Spina

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Nancy Johnson

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Ellen Steinbart

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Chang-En Yu

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Christopher M Clark

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Andrew Kertesz

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David Mann

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Ian R Mackenzie

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Thomas Bird

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Ron Petersen

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publication date

1 October 2007

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Lancet Neurology

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Clinical and pathological diagnosis of frontotemporal dementia: report of the Work Group on Frontotemporal Dementia and Pick's Disease

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Frontotemporal dementia.

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Identifiers

10.1016/S1474-4422(07)70221-1

1 reference

Europe PubMed Central

19 April 2018

http://europepmc.org/abstract/MED/17826340

1 reference

Europe PubMed Central

19 April 2018

http://europepmc.org/abstract/MED/17826340

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