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  • Men with FMR1 premutation alleles of less than 71 CGG repeats have low risk of being affected with fragile X-associated tremor/ataxia syndrome (FXTAS)

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Cognitive and behavioural genetics
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Men with FMR1 premutation alleles of less than 71 CGG repeats have low risk of being affected with fragile X-associated tremor/ataxia syndrome (FXTAS)

Authors

  • Ellenore M Martin Genetics of Learning Disability (GOLD) Service, Hunter Genetics, Newcastle, New South Wales, Australia PubMed articlesGoogle scholar articles
  • Ying Zhu Genetics of Learning Disability (GOLD) Service, Hunter Genetics, Newcastle, New South Wales, Australia Randwick Genomics Laboratory, NSW Health Pathology, Prince of Wales Hospital, Randwick, New South Wales, Australia PubMed articlesGoogle scholar articles
  • Claudine M Kraan Diagnosis and Development, Murdoch Children’s Research Institute, Royal Children’s Hospital, Melbourne, Victoria, Australia Department of Paediatrics, The University of Melbourne Faculty of Medicine Dentistry and Health Sciences, Parkville, Victoria, Australia PubMed articlesGoogle scholar articles
  • Kishore R Kumar Molecular Medicine Laboratory and Neurology Department, Concord Repatriation General Hospital, Concord Clinical School, The University of Sydney, Sydney, New South Wales, Australia Kinghorn Centre for Clinical Genomics, Garvan Institute of Medical Research, Darlinghurst, New South Wales, Australia PubMed articlesGoogle scholar articles
  • David E Godler Diagnosis and Development, Murdoch Children’s Research Institute, Royal Children’s Hospital, Melbourne, Victoria, Australia Department of Paediatrics, The University of Melbourne Faculty of Medicine Dentistry and Health Sciences, Parkville, Victoria, Australia PubMed articlesGoogle scholar articles
  • Michael Field Genetics of Learning Disability (GOLD) Service, Hunter Genetics, Newcastle, New South Wales, Australia PubMed articlesGoogle scholar articles
  1. Correspondence to Ms Ellenore M Martin, Genetics of Learning Disability (GOLD) Service, Hunter Genetics, Newcastle, New South Wales, Australia; ellenore.martin{at}health.nsw.gov.au
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Citation

Martin EM, Zhu Y, Kraan CM, et al
Men with FMR1 premutation alleles of less than 71 CGG repeats have low risk of being affected with fragile X-associated tremor/ataxia syndrome (FXTAS)
Journal of Medical Genetics 2022;59:706-709.

Publication history

  • Received February 1, 2021
  • Accepted June 27, 2021
  • First published July 28, 2021.
Online issue publication 
June 27, 2022

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© Author(s) (or their employer(s)) 2022. No commercial re-use. See rights and permissions. Published by BMJ.