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Items: 6

1.

Congenital hypomyelinating neuropathy with lethal conduction failure in mice carrying the Egr2 I268N mutation.

Baloh RH, Strickland A, Ryu E, Le N, Fahrner T, Yang M, Nagarajan R, Milbrandt J.

J Neurosci. 2009 Feb 25;29(8):2312-21. doi: 10.1523/JNEUROSCI.2168-08.2009.

2.

Molecular genetics of autosomal-dominant demyelinating Charcot-Marie-Tooth disease.

Houlden H, Reilly MM.

Neuromolecular Med. 2006;8(1-2):43-62. Review.

PMID:
16775366
3.

Regulation of myelin-specific gene expression. Relevance to CMT1.

Kamholz J, Awatramani R, Menichella D, Jiang H, Xu W, Shy M.

Ann N Y Acad Sci. 1999 Sep 14;883:91-108. Review.

PMID:
10586235
4.
5.

Demyelinating and axonal features of Charcot-Marie-Tooth disease with mutations of myelin-related proteins (PMP22, MPZ and Cx32): a clinicopathological study of 205 Japanese patients.

Hattori N, Yamamoto M, Yoshihara T, Koike H, Nakagawa M, Yoshikawa H, Ohnishi A, Hayasaka K, Onodera O, Baba M, Yasuda H, Saito T, Nakashima K, Kira J, Kaji R, Oka N, Sobue G; Study Group for Hereditary Neuropathy in Japan.

Brain. 2003 Jan;126(Pt 1):134-51. Review.

PMID:
12477701
6.

[Molecular basis of Charcot-Marie-Tooth neuropathy].

Hayasaka K.

Nihon Rinsho. 1996 Aug;54(8):2243-51. Review. Japanese.

PMID:
8810804

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