Inherited demyelinating neuropathies with micromutations of peripheral myelin protein 22 gene-Reference-Cited by-同舟云学术

Inherited demyelinating neuropathies with micromutations of peripheral myelin protein 22 gene

Published:2011-01-19 Issue:2 Volume:134 Page:608-617
ISSN:1460-2156
Container-title:Brain
language:en
Short-container-title:

Author:

Taioli Federica,Cabrini Ilaria,Cavallaro Tiziana,Acler Michele,Fabrizi Gian Maria

Publisher

Oxford University Press (OUP)

Subject

Neurology (clinical)

Link

http://academic.oup.com/brain/article-pdf/134/2/608/17347015/awq374.pdf

Reference20 articles.

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3. An abnormal mRNA produced by a novel PMP22 splice site mutation associated with HNPP;Bellone;J Neurol Neurosurg Psychiatr,2006

4. Mutational analysis of the MPZ, PMP22 and Cx32 genes in patients of Spanish ancestry with Charcot-Marie-Tooth disease and hereditary neuropathy with liability to pressure palsies;Bort;Hum Genet,1997

5. Charcot-Marie-Tooth disease and related peripheral neuropathies: novel mutations in the peripheral myelin genes connexin 32 (Cx32), peripheral myelin protein 22 (PMP22) and peripheral myelin protein zero (MPZ);Ekici;Neurogenetics,2000

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