Literature DB >> 10586271

The autosomal recessive form of CMT disease linked to 5q31-q33.

A Guilbot1, M Kessali, N Ravisé, T Hammadouche, A Bouhouche, T Maisonobe, D Grid, A Brice, E LeGuern.   

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Year:  1999        PMID： 10586271

Source DB:  PubMed          Journal:  Ann N Y Acad Sci        ISSN： 0077-8923            Impact factor:   5.691


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  2 in total

Review 1.  Autosomal-recessive forms of demyelinating Charcot-Marie-Tooth disease.

Authors:  O Dubourg; H Azzedine; C Verny; G Durosier; N Birouk; R Gouider; M Salih; A Bouhouche; A Thiam; D Grid; M Mayer; M Ruberg; M Tazir; A Brice; E LeGuern
Journal:  Neuromolecular Med       Date:  2006       Impact factor: 3.843

2.  SH3TC2/KIAA1985 protein is required for proper myelination and the integrity of the node of Ranvier in the peripheral nervous system.

Authors:  Estelle Arnaud; Jennifer Zenker; Anne-Sophie de Preux Charles; Claudia Stendel; Andreas Roos; Jean-Jacques Médard; Nicolas Tricaud; Henning Kleine; Bernhard Luscher; Joachim Weis; Ueli Suter; Jan Senderek; Roman Chrast
Journal:  Proc Natl Acad Sci U S A       Date:  2009-09-29       Impact factor: 11.205
  2 in total

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