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Chapter 53 - Déjérine–Sottas Disease

from Disorders of Infancy

Published online by Cambridge University Press:  28 April 2017

Juan M. Pascual
Juan M. Pascual
Affiliation:
University of Texas Southwestern Medical Center, Dallas
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Progressive Brain Disorders in Childhood , pp. 204 - 207
Publisher: Cambridge University Press
Print publication year: 2017

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References

Choi, Y.J., Hyun, Y.S., Nam, S.H., et al. (2015). Novel compound heterozygous nonsense PRX mutations in a Korean Dejerine-Sottas neuropathy family. J Clin Neurol. 11(1):92–6.CrossRefGoogle Scholar
Jani-Acsadi, A., Ounpuu, S., Pierz, K., et al. (2015). Pediatric Charcot-Marie-tooth disease. Pediatr Clin North Am. 62(3):767–86.CrossRefGoogle ScholarPubMed

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  • Déjérine–Sottas Disease
  • Juan M. Pascual, University of Texas Southwestern Medical Center, Dallas
  • Book: Progressive Brain Disorders in Childhood
  • Online publication: 28 April 2017
  • Chapter DOI: https://doi.org/10.1017/9781107323704.054
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  • Déjérine–Sottas Disease
  • Juan M. Pascual, University of Texas Southwestern Medical Center, Dallas
  • Book: Progressive Brain Disorders in Childhood
  • Online publication: 28 April 2017
  • Chapter DOI: https://doi.org/10.1017/9781107323704.054
Available formats
×

Save book to Google Drive

To save content items to your account, please 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 account. Find out more about saving content to Google Drive.

  • Déjérine–Sottas Disease
  • Juan M. Pascual, University of Texas Southwestern Medical Center, Dallas
  • Book: Progressive Brain Disorders in Childhood
  • Online publication: 28 April 2017
  • Chapter DOI: https://doi.org/10.1017/9781107323704.054
Available formats
×