Evidence for the role ofFMR1gray zone alleles as a risk factor for parkinsonism in females-Reference-Cited by-同舟云学术

Evidence for the role ofFMR1gray zone alleles as a risk factor for parkinsonism in females

Published:2018-07 Issue:7 Volume:33 Page:1178-1181
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Mov Disord.

Author:

Loesch Danuta Z.¹^ORCID,Tassone Flora²,Mellick George D.³,Horne Malcolm⁴,Rubio Justin P.⁴⁵,Bui Minh Q.⁶,Francis David⁷,Storey Elsdon⁸

Affiliation:

1. Department of Psychology and Counselling; School of Psychology and Public Health, College of Science Health and Engineering, La Trobe University; Melbourne VIC Australia

2. UC Davis MIND Institute; Sacramento California USA

3. Griffith Institute for Drug Discovery; Griffith University; Brisbane Queensland Australia

4. The Florey Institute of Neuroscience and Mental Health; Melbourne VIC Australia

5. Department of Pharmacology and Therapeutics; University of Melbourne; VIC Australia

6. Centre for Epidemiology and Biostatistics; Melbourne School of Population and Global Health, University of Melbourne; VIC Australia

7. Victorian Clinical Genetic Services; Melbourne VIC Australia

8. Department of Medicine (Neuroscience); Monash University (Alfred Hospital Campus); Melbourne VIC Australia

Funder

The National Institutes of Child Health and Human Development Grant

Brain Foundation Research Grant

Bethlehem Griffiths Research Foundation Grant

Victorian Clinical Genetic Services

Newborn Screening

CRC

Eunice Kennedy Shriver National Institute of Child Health and Human Development

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/mds.27420/fullpdf

Reference30 articles.

1. Parkinsonian Disorders in Clinical Practice

2. The relationship between glucocerebrosidase mutations and Parkinson disease;Migdalska-Richards;J Neurochem,2016

3. Small CGG repeat expansion alleles of FMR1 gene are associated with parkinsonism;Loesch;Clin Genet,2009

4. New evidence for, and challenges in, linking small CGG repeat expansion FMR1 alleles with Parkinson's disease;Loesch;Clin Genet,2013

5. Accuracy of clinical diagnosis of idiopathic Parkinson's disease. A clinico-pathological study of 100 cases;Hughes;JNNP,1992

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