Synapse
⌘+K
Synapse
PulseExploreClubsResearchersJournals
Instagram
HomeClubsExplore
February 2, 2008Brain

Phenotype variability in progranulin mutation carriers: a clinical, neuropsychological, imaging and genetic study

View Full Paper
Ask AI
Bookmark
Share

Authors

IBIsabelle Le BerCentre National de la Recherche ScientifiqueACAgnès CamuzatCentre National de la Recherche ScientifiqueDHDidier HannequinUniversité Claude Bernard Lyon 1

Discussion

Loading...

Member takes

Implication

Key Points

Key points are not available for this paper at this time.

Cite This Study

Ber et al. (2008) studied this question.

synapsesocial.com/papers/6a7cc32f178e986690cf8a1ahttps://doi.org/10.1093/brain/awn012
View Full Paper
Ask AI
Bookmark
Share

Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1The Neuropsychiatric Inventory1994 · 7,648 citations
  2. 2Progranulin gene mutations associated with frontotemporal dementia and progressive non-fluent aphasia2006 · 201 citations
  3. 3Characteristics of frontotemporal dementia patients with a Progranulin mutation2006 · 88 citations
  4. 4Neuropathologic Features of Frontotemporal Lobar Degeneration With Ubiquitin-Positive Inclusions With Progranulin Gene (PGRN) Mutations2007 · 185 citations
  5. 5Progranulin mutations and amyotrophic lateral sclerosis or amyotrophic lateral sclerosis-frontotemporal dementia phenotypes2006 · 134 citations