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Novel double deletions in the MECP2 gene in Tunisian Rett patient.
Fendri-Kriaa N, Rouissi A, Ghorbel R, Mkaouar-Rebai E, Belguith N, Gouider-Khouja N, Fakhfakh F. Fendri-Kriaa N, et al. Gene. 2012 Jul 10;502(2):163-7. doi: 10.1016/j.gene.2012.04.028. Epub 2012 Apr 25. Gene. 2012. PMID: 22561697
Hypomyelination and Congenital Cataract: Clinical, Imaging, and Genetic Findings in Three Tunisian Families and Literature Review.
Kraoua I, Bouyacoub Y, Drissi C, Chargui M, Rebai I, Chebil A, Klaa H, Benrhouma H, Hassen A, Gouider-Khouja N, Abdelhak S, Boespflug-Tanguy O, Youssef-Turki IB, Dorboz I. Kraoua I, et al. Among authors: gouider khouja n. Neuropediatrics. 2021 Aug;52(4):302-309. doi: 10.1055/s-0041-1728654. Epub 2021 Jun 30. Neuropediatrics. 2021. PMID: 34192786 Review.
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 R, Ghorbel R, Rouissi A, Fendri-Kriaa N, Ben Salah G, Belguith N, Ammar-Keskes L, Gouider-Khouja N, Fakhfakh F. Ghorbel R, et al. Among authors: gouider khouja n. Biochem Biophys Res Commun. 2018 Feb 26;497(1):93-101. doi: 10.1016/j.bbrc.2018.02.029. Epub 2018 Feb 6. Biochem Biophys Res Commun. 2018. PMID: 29421650
Status dystonicus in childhood.
Touati N, Ben Rhouma H, Kraoua I, Klaa H, Turki I, Gouider-Khouja N. Touati N, et al. Among authors: gouider khouja n. Tunis Med. 2015 Dec;93(12):756-9. Tunis Med. 2015. PMID: 27249384 Free article.
58 results