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New evidence for, and challenges in, linking small CGG repeat expansion FMR1 alleles with Parkinson's disease

  1. DZ Loesch1,*,
  2. F Tassone2,3,
  3. J Lo2,
  4. HR Slater4,
  5. LV Hills4,
  6. MQ Bui5,
  7. PA Silburn6,
  8. GD Mellick7

Article first published online: 25 DEC 2012

DOI: 10.1111/cge.12070

Additional Information

How to Cite

Loesch DZ, Tassone F, Lo J, Slater HR, Hills LV, Bui MQ, Silburn PA, Mellick GD. New evidence for, and challenges in, linking small CGG repeat expansion FMR1 alleles with Parkinson's disease.

Author Information

  1. 1

    School of Psychological Science, La Trobe University, Bundoora, Victoria, Australia

  2. 2

    Department of Biochemistry and Molecular Medicine, School of Medicine, University of California Davis, Davis, CA, USA

  3. 3

    Medical Investigation of Neurodevelopmental Disorders (M.I.N.D.) Institute, University of California Davis Medical Center, Sacramento, CA, USA

  4. 4

    VCGS Cytogenetics Laboratory, Murdoch Childrens Research Institute, Royal Children's Hospital, Parkville, Australia

  5. 5

    Centre for Molecular, Environmental, Genetic, and Analytic Epidemiology, University of Melbourne, Parkville, Victoria, Australia

  6. 6

    Centre for Clinical Research, University of Queensland, Herston, Australia

  7. 7

    Eskitis Institute for Cell and Molecular Therapies, Griffith University, Queensland, Brisbane, Australia

* Corresponding author: Dr Danuta Loesch, School of Psychological Science, La Trobe University, Bundoora, Victoria 3086, Australia.
Tel.: +61 3 94791382;
fax: +61 3 94791956;
e-mail: d.loesch@latrobe.edu.au

  1. Nothing to declare.

Publication History

  1. Article first published online: 25 DEC 2012
  2. Accepted manuscript online: 30 NOV 2012 12:09PM EST
  3. Manuscript Revised: 19 NOV 2012
  4. Manuscript Accepted: 19 NOV 2012
  5. Manuscript Received: 20 SEP 2012

Funded by

  • National Institutes of Child Health and Human Development. Grant Number: 36071
  • NHMRC project. Grant Number: 330400

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