X-linked Charcot-Marie-Tooth disease-Reference-Cited by-同舟云学术

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X-linked Charcot-Marie-Tooth disease

Published:1991-01 Issue:1 Volume:87 Page:23-27
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Mostacciuolo M. L.,M�ller E.,Fardin P.,Micaglio G. F.,Bardoni B.,Guioli S.,Camerino G.,Danieli G. A.

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/BF01213086.pdf

Reference14 articles.

1. Arveiler B, Oberlé I, Mandel JL (1987) Genetic mapping of nine DNA markers in the q11?q22 region of the human X chromosome. Genomics 1:60?66

2. Beckett J, Holden NE, Simson BN, White BN, MacLeod PM (1986) Localization of X-linked dominant Charcot-Marie-Tooth disease (CMT 2) to Xq13. J Neurogenet 3:225?231

3. De Saint Basile G, Arveiler B, Malcom S, Levinsky RJ, Lau YL, Hofker M, Debre M, Fischer A, Griscelli C, Mandel JL (1987) Close linkage of the locus for X chromosome-linked severe combined immunodeficiency to polymorphic DNA markers in Xq11?13. Proc Natl Acad Sci USA 84:7576?7579

4. Fischbeck KH, Ar-Rushdi N, Pericak-Vance M, Rozear M, Roses AD, Fryns JP (1986) X-linked neuropathy: gene localization with DNA probes. Ann Neurol 20:527?532

5. Gal A, Mucke J, Theile H, Wieacker PF, Ropers HH, Wienker TF (1985) X-linked Charcot-Marie-Tooth disease: suggestion of linkage with a cloned DNA sequence from the proximal Xq. Hum Genet 70:38?42

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1. Charcot-Marie-Tooth Disease, Type X1;Genetic Neuromuscular Disorders;2017-10-06

2. Intermediate Charcot–Marie–Tooth disease: an electrophysiological reappraisal and systematic review;Journal of Neurology;2017-03-31

3. Charcot-Marie-Tooth Disease, Type X1;Genetic Neuromuscular Disorders;2014

4. Charcot–Marie–Tooth Disease;Gap Junctions in the Brain;2013

5. Identification of the variant Ala335Val of MED25 as responsible for CMT2B2: molecular data, functional studies of the SH3 recognition motif and correlation between wild-type MED25 and PMP22 RNA levels in CMT1A animal models;neurogenetics;2009-03-17

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