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June 7, 2016BMC Research NotesOpen Access

Clinical heterogeneity of PLA2G6-related Parkinsonism: analysis of two Saudi families

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Authors

SBSaeed BohlegaBABashayer Al‐MubarakEAEman A. Alyemni

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Bohlega et al. (2016) studied this question.

synapsesocial.com/papers/6aaa3d31d8fbdcd7a1dfd8cehttps://doi.org/10.1186/s13104-016-2102-7
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Also Consider

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

  1. 1<i>PLA2G6</i> gene mutation in autosomal recessive early-onset parkinsonism in a Chinese cohort2011 · 97 citations
  2. 2Parkinson’s Disease in Saudi Patients: A Genetic Study2015 · 30 citations
  3. 3Phospholipase A<sub>2</sub>, reactive oxygen species, and lipid peroxidation in CNS pathologies2008 · 193 citations
  4. 4Characterization of PLA2G6 as a locus for dystonia‐parkinsonism2008 · 485 citations
  5. 5Catalytic Function of PLA2G6 Is Impaired by Mutations Associated with Infantile Neuroaxonal Dystrophy but Not Dystonia-Parkinsonism2010 · 121 citations