(Q54427566)

29 May 2018

title

Genetic epidemiology of Charcot-Marie-Tooth in the general population. (English)

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29 May 2018

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G J Braathen

1

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J C Sand

2

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A Lobato

3

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H Høyer

4

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M B Russell

5

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publication date

1 January 2011

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29 May 2018

European Journal of Neurology

published in

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29 May 2018

volume

18

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issue

1

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page(s)

39-48

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29 May 2018

Lower motor and primary sensory neuron diseases with peroneal muscular atrophy. I. Neurologic, genetic, and electrophysiologic findings in hereditary polyneuropathies

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Mutational analysis of PMP22, MPZ, GJB1, EGR2 and NEFL in Korean Charcot-Marie-Tooth neuropathy patients

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Effectiveness of real-time quantitative PCR compare to repeat PCR for the diagnosis of Charcot-Marie-Tooth Type 1A and hereditary neuropathy with liability to pressure palsies

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Two novel connexin32 mutations cause early onset X-linked Charcot-Marie-Tooth disease

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Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A

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MFN2 point mutations occur in 3.4% of Charcot-Marie-Tooth families. An investigation of 232 Norwegian CMT families

21 January 2018

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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

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Identifiers

DOI

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29 May 2018

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29 May 2018