Skip to main content Accessibility help
×
Home

A Novel Exon 3 Mutation (P66S) in the SOD1 Gene in Familial ALS

  • Wonki Baek (a1), Seong-Ho Koh (a1), Young Seo Kim (a1), Hyun Young Kim (a1), Min-Jung Kwon (a2), Chang-Seok Ki (a3) and Seung Hyun Kim (a1)...
    • Send article to Kindle

      To send this article to your Kindle, first ensure no-reply@cambridge.org is added to your Approved Personal Document E-mail List under your Personal Document Settings on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part of your Kindle email address below. Find out more about sending to your Kindle. Find out more about sending to your Kindle.

      Note you can select to send to either the @free.kindle.com or @kindle.com variations. ‘@free.kindle.com’ emails are free but can only be sent to your device when it is connected to wi-fi. ‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.

      Find out more about the Kindle Personal Document Service.

      A Novel Exon 3 Mutation (P66S) in the SOD1 Gene in Familial ALS
      Available formats
      ×

      Send article to Dropbox

      To send this article to your Dropbox account, please select one or more formats and confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your <service> account. Find out more about sending content to Dropbox.

      A Novel Exon 3 Mutation (P66S) in the SOD1 Gene in Familial ALS
      Available formats
      ×

      Send article to Google Drive

      To send this article to your Google Drive account, please select one or more formats and confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your <service> account. Find out more about sending content to Google Drive.

      A Novel Exon 3 Mutation (P66S) in the SOD1 Gene in Familial ALS
      Available formats
      ×

Abstract

  • An abstract is not available for this content so a preview has been provided below. To view the full text please use the links above to select your preferred format.

Copyright

Corresponding author

Department of Neurology, Hanyang University Hospital, 17 Haengdang-dong, Seongdong-gu, Seoul 133-792, South Korea.

References

Hide All
1Rosen, DR.Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis. Nature. 1993;364:362.
2Segovia-Silvestre, T, Andreu, AL, Vives-Bauza, C, Garcia-Arumi, E, Cervera, C, Gamez, J.A novel exon 3 mutation (D76V) in the SOD1 gene associated with slowly progressive ALS. Amyotroph Lateral Scler Other Motor Neuron Disord. 2002;3:6974.
3Giess, R, Holtmann, B, Braga, M, et al.Early onset of severe familial amyotrophic lateral sclerosis with a SOD-1 mutation: potential impact of CNTF as a candidate modifier gene. Am J Hum Genet. 2002;70:127786.
4del Grande, ALuigetti, MConte, A, et al.A novel L67P SOD1 mutation in an Italian ALS patient. Amyotroph Lateral Scler. 2011;12:1502.
5Radunovic, A, Leigh, PN.Cu/Zn superoxide dismutase gene mutations in amyotrophic lateral sclerosis: correlation between genotype and clinical features. J Neurol Neurosurg Psychiatry. 1996;61:56572.

Metrics

Full text views

Total number of HTML views: 0
Total number of PDF views: 0 *
Loading metrics...

Abstract views

Total abstract views: 0 *
Loading metrics...

* Views captured on Cambridge Core between <date>. This data will be updated every 24 hours.

Usage data cannot currently be displayed