Literature DB >> 25414040

Reply: PRKAR1B mutations are a rare cause of FUS negative neuronal intermediate filament inclusion disease.

Tsz Hang Wong1, Annemieke J M H Verkerk2, Annemieke J Rozemuller3, Rob Willemsen4, Manuela Neumann5, Vincenzo Bonifati4, John van Swieten6.   

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Year:  2014        PMID： 25414040      PMCID： PMC4614125          DOI： 10.1093/brain/awu333

Source DB:  PubMed          Journal:  Brain        ISSN： 0006-8950            Impact factor:   13.501


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  3 in total

1.  PRKAR1B mutations are a rare cause of FUS negative neuronal intermediate filament inclusion disease.

Authors:  Cyril Pottier; Matt Baker; Dennis W Dickson; Rosa Rademakers
Journal:  Brain       Date:  2014-11-20       Impact factor: 13.501

2.  PRKAR1B mutation associated with a new neurodegenerative disorder with unique pathology.

Authors:  Tsz Hang Wong; Wang Zheng Chiu; Guido J Breedveld; Ka Wan Li; Annemieke J M H Verkerk; David Hondius; Renate K Hukema; Harro Seelaar; Petra Frick; Lies-Anne Severijnen; Gert-Jan Lammers; Joyce H G Lebbink; Sjoerd G van Duinen; Wouter Kamphorst; Annemieke J Rozemuller; E Bert Bakker; Manuela Neumann; Rob Willemsen; Vincenzo Bonifati; August B Smit; John van Swieten
Journal:  Brain       Date:  2014-04-09       Impact factor: 13.501

3.  Mutation frequency of PRKAR1B and the major familial dementia genes in a Dutch early onset dementia cohort.

Authors:  P E Cohn-Hokke; T H Wong; P Rizzu; G Breedveld; W M van der Flier; P Scheltens; F Baas; P Heutink; E J Meijers-Heijboer; J C van Swieten; Y A L Pijnenburg
Journal:  J Neurol       Date:  2014-08-10       Impact factor: 4.849
  3 in total

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