The C9orf72 hexanucleotide repeat expansion presents a challenge for testing laboratories and genetic counseling-Reference-Cited by-同舟云学术

The C9orf72 hexanucleotide repeat expansion presents a challenge for testing laboratories and genetic counseling

Published:2019-03-23 Issue:5-6 Volume:20 Page:310-316
ISSN:2167-8421
Container-title:Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration
language:en
Short-container-title:Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration

Author:

Crook Ashley¹²³^ORCID,McEwen Alison³^ORCID,Fifita Jennifer A.²^ORCID,Zhang Katharine²,Kwok John B.⁴⁵^ORCID,Halliday Glenda⁴^ORCID,Blair Ian P.²^ORCID,Rowe Dominic B.¹²^ORCID

Affiliation:

1. Department of Clinical Medicine, Faculty of Medicine and Health Sciences, Macquarie University, Sydney, Australia,

2. Centre for MND Research, Department of Biomedical Science, Faculty of Medicine and Health Sciences, Macquarie University, Sydney, Australia,

3. Graduate School of Health, University of Technology Sydney, Ultimo, Australia,

4. Central Clinical School and Brain and Mind Centre, The University of Sydney, Sydney, Australia,

5. School of Medical Sciences, University of New South Wales, Sydney, Australia

Funder

National Health and Medical Research Council of Australia

NHMRC

Publisher

Informa UK Limited

Subject

Clinical Neurology,Neurology

Link

https://www.tandfonline.com/doi/pdf/10.1080/21678421.2019.1588904

Reference60 articles.

1. Genetics of dementia: Update and guidelines for the clinician

2. Genetic testing and genetic counseling for amyotrophic lateral sclerosis: an update for clinicians

3. Genetic screening in sporadic ALS and FTD

4. Patients with sporadic and familial amyotrophic lateral sclerosis found value in genetic testing

5. Patients with Amyotrophic Lateral Sclerosis Have High Interest in and Limited Access to Genetic Testing

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