Literature DB >> 15770224

Mutations in exon 1 of MECP2B are not a common cause of X-linked mental retardation in males.

Karine Poirier, Fiona Francis, Ben Hamel, Claude Moraine, Jean Pierre Fryns, Hans H Ropers, Jamel Chelly, Thierry Bienvenu.   

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Year:  2005        PMID： 15770224     DOI： 10.1038/sj.ejhg.5201399

Source DB:  PubMed          Journal:  Eur J Hum Genet        ISSN： 1018-4813            Impact factor:   4.246


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  3 in total

Review 1.  X linked mental retardation: a clinical guide.

Authors:  F L Raymond
Journal:  J Med Genet       Date:  2005-08-23       Impact factor: 6.318

Review 2.  MECP2 mutations in males.

Authors:  Laurent Villard
Journal:  J Med Genet       Date:  2007-03-09       Impact factor: 6.318

3.  The first missense mutation causing Rett syndrome specifically affecting the MeCP2_e1 isoform.

Authors:  Yann Fichou; Juliette Nectoux; Nadia Bahi-Buisson; Haydeé Rosas-Vargas; Benoit Girard; Jamel Chelly; Thierry Bienvenu
Journal:  Neurogenetics       Date:  2008-11-26       Impact factor: 2.660
  3 in total

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