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Search: WFRF:(Elder G) > (2005-2009) > Progranulin mutatio...

Progranulin mutations and amyotrophic lateral sclerosis or amyotrophic lateral sclerosis-frontotemporal dementia phenotypes.

Schymick, J C (author)
Yang, Y (author)
Andersen, P M (author)
Umeå universitet,Neurologi
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Vonsattel, J P (author)
Greenway, M (author)
Momeni, P (author)
Elder, J (author)
Chiò, A (author)
Restagno, G (author)
Robberecht, W (author)
Dahlberg, C (author)
Karolinska Institutet
Mukherjee, O (author)
Goate, A (author)
Graff-Radford, N (author)
Caselli, R J (author)
Hutton, M (author)
Gass, J (author)
Cannon, A (author)
Rademakers, R (author)
Singleton, A B (author)
Hardiman, O (author)
Rothstein, J (author)
Hardy, J (author)
Traynor, B J (author)
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 (creator_code:org_t)
2006-12-18
2007
English.
In: J Neurol Neurosurg Psychiatry. - : BMJ. - 1468-330X .- 0022-3050. ; 78:7, s. 754-6
  • Journal article (other academic/artistic)
Subject headings
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Keyword

Adult
Aged
Aged; 80 and over
Amyotrophic Lateral Sclerosis/*complications/*genetics
Cross-Sectional Studies
DNA Mutational Analysis
Dementia/*etiology/*genetics
Female
Humans
Intercellular Signaling Peptides and Proteins/*genetics
Male
Middle Aged
Mutation; Missense
Phenotype

Publication and Content Type

vet (subject category)
art (subject category)

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