Literature DB >> 12481990

De novo MECP2 mutation in a 46,XX male patient with Rett syndrome.

Robert Maiwald, Anselm Bönte, Helena Jung, Pavel Bitter, Zoe Storm, Franco Laccone, Peter Herkenrath.   

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Year:  2002        PMID： 12481990     DOI： 10.1007/s10048-002-0137-5

Source DB:  PubMed          Journal:  Neurogenetics        ISSN： 1364-6745            Impact factor:   2.660


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  3 in total

Review 1.  Brief report: systematic review of Rett syndrome in males.

Authors:  Brian Reichow; Annie George-Puskar; Tara Lutz; Isaac C Smith; Fred R Volkmar
Journal:  J Autism Dev Disord       Date:  2015-10

Review 2.  MECP2 mutations in males.

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

3.  Regulatory functions and pathological relevance of the MECP2 3'UTR in the central nervous system.

Authors:  Heather McGowan; Zhiping P Pang
Journal:  Cell Regen (Lond)       Date:  2015-10-28
  3 in total

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