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Aida Rouissi
Aida Rouissi
Rett syndrome
Neurodevelopmental disorder
Genetics
Point mutation
MECP2
2
Papers
3
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0
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Novel mutations in the C-terminal region of the MECP2 gene in Tunisian Rett syndrome patients.
2012
Journal of Child Neurology
Nourhene Fendri-Kriaa
Aida Rouissi
Rania Ghorbel
Emna Mkaouar-Rebai
Neila Belguith
Naziha Gouider-Khouja
Faiza Fakhfakh
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Novel double deletions in the MECP2 gene in Tunisian Rett patient
2012
Gene
Nourhene Fendri-Kriaa
Aida Rouissi
Rania Ghorbel
Emna Mkaouar-Rebai
Neila Belguith
Naziha Gouider-Khouja
Faiza Fakhfakh
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Citations (2)
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