Disruption of neurofilament network with aggregation of light neurofilament protein: a common pathway leading to motor neuron degeneration due to Charcot–Marie–Tooth disease-linked mutations in NFL and HSPB1-Reference-Cited by-同舟云学术

Disruption of neurofilament network with aggregation of light neurofilament protein: a common pathway leading to motor neuron degeneration due to Charcot–Marie–Tooth disease-linked mutations in NFL and HSPB1

Published:2007-09-19 Issue:24 Volume:16 Page:3103-3116
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Zhai Jinbin,Lin Hong,Julien Jean-Pierre,Schlaepfer William W.

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/16/24/3103/13917214/ddm272.pdf

Reference58 articles.

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2. Disease mechanisms in inherited neuropathies;Suter;Nat. Rev. Neurosci.,2003

3. A new variant of Charcot–Marie–Tooth disease type 2 is probably the result of a mutation in the neurofilament-light gene;Mersiyanova;Am. J. Hum. Genet.,2000

4. Further evidence that neurofilament light chain gene mutations can cause Charcot–Marie–Tooth disease type 2E;De Jonghe;Ann. Neurol.,2001

5. Mutations in the neurofilament light chain gene (NEFL) cause early onset severe Charcot–Marie–Tooth disease;Jordanova;Brain,2003

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