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December 11, 2002Brain

Haploinsufficiency at the -synuclein gene underlies phenotypic severity in familial Parkinson's disease

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Authors

HKHirokazu KobayashiKyushu UniversityRKRejko KrügerCentre Hospitalier de LuxembourgKMKaterina MarkopoulouNorthShore University HealthSystem

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Kobayashi et al. (2002) studied this question.

synapsesocial.com/papers/6ab629c60a2a2fa37dfb893fhttps://doi.org/10.1093/brain/awg010
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Also Consider

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

  1. 1Mutated α-synuclein gene in two Greek kindreds with familial PD: Incomplete penetrance?1999 · 134 citations
  2. 2Fibrils Formed in Vitro from α-Synuclein and Two Mutant Forms Linked to Parkinson's Disease are Typical Amyloid2000 · 795 citations
  3. 3Synthetic filaments assembled from C‐terminally truncated α‐synuclein1998 · 425 citations
  4. 4α-Synuclein in filamentous inclusions of Lewy bodies from Parkinson’s disease and dementia with Lewy bodies1998 · 3,248 citations
  5. 5Proteome analysis of polyacrylamide gel-separated proteins visualized by reversible negative staining using imidazole-zinc salts1999 · 65 citations