First report of an unusual novel double mutation affecting...

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Biochemical and Biophysical Research Communications 2018 / 2

First report of an unusual novel double mutation affecting the transcription repression domain of MeCP2 and causing a severe phenotype of Rett syndrome: Molecular analyses and computational investigation

Ghorbel, Rania, Ghorbel, Raouia, Rouissi, Aida, Fendri-Kriaa, Nourhene, Ben Salah, Ghada, Belguith, Neila, Ammar-Keskes, Leila, Gouider-Khouja, Neziha, Fakhfakh, Faiza
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Language:
english
Journal:
Biochemical and Biophysical Research Communications
DOI:
10.1016/j.bbrc.2018.02.029
Date:
February, 2018
File:
PDF, 1.77 MB
english, 2018
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