Literature DB >> 20108394

Novel human pathological mutations. Gene symbol: MECP2. Disease: Rett Syndrome.

Rajni Khajuria1, Savita Sapra, Manju Ghosh, Neerja Gupta, Sheffali Ghulati, Veena Kalra, Madhulika Kabra.   

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Year:  2010        PMID： 20108394

Source DB:  PubMed          Journal:  Hum Genet        ISSN： 0340-6717            Impact factor:   4.132


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  1 in total

Review 1.  Novel therapeutic approaches: Rett syndrome and human induced pluripotent stem cell technology.

Authors:  Mohan Gomathi; Vellingiri Balachandar
Journal:  Stem Cell Investig       Date:  2017-03-02
  1 in total

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