Diagnostic laboratory testing for Charcot Marie Tooth disease (CMT): the spectrum of gene defects in Norwegian patients with CMT and its implications for future genetic test strategies-Reference-Cited by-同舟云学术

Diagnostic laboratory testing for Charcot Marie Tooth disease (CMT): the spectrum of gene defects in Norwegian patients with CMT and its implications for future genetic test strategies

Published:2013-09-21 Issue:1 Volume:14 Page:
ISSN:1471-2350
Container-title:BMC Medical Genetics
language:en
Short-container-title:BMC Med Genet

Author:

Østern Rune,Fagerheim Toril,Hjellnes Helene,Nygård Bjørn,Mellgren Svein I,Nilssen Øivind

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1186/1471-2350-14-94.pdf

Reference26 articles.

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3. Harding AE, Thomas PK: The clinical features of hereditary motor and sensory neuropathy types I and II. Brain. 1980, 103: 259-280. 10.1093/brain/103.2.259.

4. Nicholson G, Myers S: Intermediate forms of Charcot-Marie-Tooth neuropathy: a review. Neuromolecular Med. 2006, 8: 123-130.

5. Bird TD: Charcot-Marie-Tooth Hereditary Neuropathy Overview. 2012, Gene Reviews (accessed June 02, 2012), [ http://www.ncbi.nlm.nih.gov/books/NBK1358/ ]

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