A transgenic rat model of Charcot-Marie-Tooth disease (Q71078153)

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16 October 2019

title

A transgenic rat model of Charcot-Marie-Tooth disease (English)

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16 October 2019

M Sereda

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16 October 2019

I Griffiths

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16 October 2019

A Pühlhofer

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16 October 2019

H Stewart

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16 October 2019

M J Rossner

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16 October 2019

F Zimmerman

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16 October 2019

J P Magyar

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16 October 2019

A Schneider

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16 October 2019

E Hund

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16 October 2019

H M Meinck

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16 October 2019

U Suter

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16 October 2019

K A Nave

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16 October 2019

publication date

1 May 1996

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16 October 2019

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16 October 2019

volume

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16 October 2019

issue

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16 October 2019

page(s)

1049-1060

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Hypermyelination and demyelinating peripheral neuropathy in Pmp22-deficient mice

16 October 2019

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Connexin mutations in X-linked Charcot-Marie-Tooth disease

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Charcot–Marie–Tooth neuropathy type 1B is associated with mutations of the myelin P0 gene

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Nerve conduction studies in Charcot-Marie-Tooth polyneuropathy associated with a segmental duplication of chromosome 17

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Peripheral myelin protein-22 gene maps in the duplication in chromosome 17p11.2 associated with Charcot-Marie-Tooth 1A.

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The effects of cAMP on differentiation of cultured Schwann cells: progression from an early phenotype (04+) to a myelin phenotype (P0+, GFAP-, N-CAM-, NGF-receptor-) depends on growth inhibition

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7 January 2021

Charcot-Marie-Tooth disease: a new paradigm for the mechanism of inherited disease

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7 January 2021

The gene for the peripheral myelin protein PMP-22 is a candidate for Charcot-Marie-Tooth disease type 1A

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7 January 2021

Duplication in chromosome 17p11.2 in Charcot-Marie-Tooth neuropathy type 1a (CMT 1a)

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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Identifiers

DOI

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16 October 2019

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