Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
8294214 | Biochemical and Biophysical Research Communications | 2018 | 9 Pages |
Abstract
Therefore, this is the first study which highlights a novel double mutation among the transcription repression domain (TRD) of MeCP2 protein in Rett patient with a severe clinical phenotype in North Africa region.
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Biochemistry
Authors
Rania Ghorbel, Raouia Ghorbel, Aida Rouissi, Nourhene Fendri-Kriaa, Ghada Ben Salah, Neila Belguith, Leila Ammar-Keskes, Neziha Gouider-Khouja, Faiza Fakhfakh,