scholarly journals Correction to: Fucosidosis in Tunisian patients: mutational analysis and homology-based modeling of FUCA1 enzyme

2021 ◽  
Vol 14 (1) ◽  
Author(s):  
Latifa Chkioua ◽  
Yessine Amri ◽  
Sahli Chaima ◽  
Ferdawes Fenni ◽  
Hela Boudabous ◽  
...  
Keyword(s):  
Mutational Analysis ◽  
Tunisian Patients

An amendment to this paper has been published and can be accessed via a link at the top of the paper.

Mutational analysis of the mitochondrial 12S rRNA and tRNASer(UCN) genes in Tunisian patients with nonsyndromic hearing loss

2006 ◽  
Vol 340 (4) ◽  
pp. 1251-1258 ◽  
Author(s):  
Emna Mkaouar-Rebai ◽  
Abdelaziz Tlili ◽  
Saber Masmoudi ◽  
Nacim Louhichi ◽  
Ilhem Charfeddine ◽  
...  
Keyword(s):  
Hearing Loss ◽  
Mutational Analysis ◽  
12S Rrna ◽  
Nonsyndromic Hearing Loss ◽  
Tunisian Patients ◽  
Mitochondrial 12S Rrna

Mutational Analysis of the MECP2 Gene in Tunisian Patients With Rett Syndrome: A Novel Double Mutation

2010 ◽  
Vol 25 (8) ◽  
pp. 1042-1046 ◽  
Author(s):  
Nourhene Fendri-Kriaa ◽  
Emna Mkaouar-Rebai ◽  
Dorsaf Moalla ◽  
Neila Belguith ◽  
Nacim Louhichi ◽  
...  
Keyword(s):  
Rett Syndrome ◽  
Mutational Analysis ◽  
Mecp2 Gene ◽  
Double Mutation ◽  
Tunisian Patients

Mutational analysis of the mitochondrial tRNALeu(UUR) gene in Tunisian patients with mitochondrial diseases

2007 ◽  
Vol 355 (4) ◽  
pp. 1031-1037 ◽  
Author(s):  
Emna Mkaouar-Rebai ◽  
Abdelaziz Tlili ◽  
Saber Masmoudi ◽  
Neila Belguith ◽  
Ilhem Charfeddine ◽  
...  
Keyword(s):  
Mutational Analysis ◽  
Mitochondrial Diseases ◽  
Tunisian Patients

The co-chaperone BAG-1 as a candidate for causing cortisteroid receptor resistance: A detailed mutational analysis

2004 ◽  
Vol 36 (05) ◽  
Author(s):  
U Schmidt ◽  
M Rosenhagen ◽  
F Holsboer ◽  
T Rein
Keyword(s):  
Mutational Analysis
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