Heterogeneity within a large kindred with frontotemporal dementia: a novel progranulin mutation.
Neurology
; 69(2): 140-7, 2007 Jul 10.
Article
in En
| MEDLINE
| ID: mdl-17620546
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Collection:
01-internacional
Database:
MEDLINE
Main subject:
Genetic Predisposition to Disease
/
Dementia
/
Intercellular Signaling Peptides and Proteins
/
Mutation
Type of study:
Etiology_studies
/
Incidence_studies
/
Observational_studies
/
Prognostic_studies
/
Risk_factors_studies
Limits:
Adult
/
Aged
/
Aged80
/
Female
/
Humans
/
Male
/
Middle aged
Country/Region as subject:
Europa
Language:
En
Journal:
Neurology
Year:
2007
Document type:
Article
Affiliation country:
Italy
Country of publication:
United States