Transgenic expression of neuronal dystonin isoform 2 partially rescues the disease phenotype of the dystonia musculorum mouse model of hereditary sensory autonomic neuropathy VI-Reference-Cited by-同舟云学术

Transgenic expression of neuronal dystonin isoform 2 partially rescues the disease phenotype of the dystonia musculorum mouse model of hereditary sensory autonomic neuropathy VI

Published:2013-12-30 Issue:10 Volume:23 Page:2694-2710
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Human Molecular Genetics

Author:

Ferrier A.,Sato T.,De Repentigny Y.,Gibeault S.,Bhanot K.,O'Meara R. W.,Lynch-Godrei A.,Kornfeld S. F.,Young K. G.,Kothary R.

Publisher

Oxford University Press (OUP)

Subject

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

Link

http://academic.oup.com/hmg/article-pdf/23/10/2694/1695475/ddt663.pdf

Reference40 articles.

1. Mechanisms of disease in hereditary sensory and autonomic neuropathies

2. Genes for hereditary sensory and autonomic neuropathies: a genotype-phenotype correlation

3. Hereditary sensory autonomic neuropathy caused by a mutation in dystonin

4. Cellular and Molecular Biology of Neuronal Dystonin

5. CLINICAL AND PATHOLOGICAL STUDIES OF AN HEREDITARY NEUROPATHY IN MICE (DYSTONIA MUSCULORUM)

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