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Wieme Maamouri-hicheri
Wieme Maamouri-hicheri
Genetics
Nonsense mutation
Biology
Autosomal recessive cerebellar ataxia
Oculomotor apraxia
2
Papers
14
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Clinical features and molecular genetics of two Tunisian families with abetalipoproteinemia
2014
Journal of Clinical Neuroscience
Monia B. Hammer
Ghada El Euch-Fayache
Houda Nehdi
Moncef Feki
Wieme Maamouri-hicheri
Fayçal Hentati
Rim Amouri
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Citations (7)
Clinical and molecular findings of ataxia with oculomotor apraxia type 2 (AOA2) in 5 Tunisian families.
2012
Diagnostic Molecular Pathology
Monia B. Hammer
Ghada El Euch-Fayache
Houda Nehdi
Dalel Saidi
Amira Nasri
Fatma Nabli
Yosr Bouhlal
Wieme Maamouri-hicheri
Fayçal Hentati
Rim Amouri
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Citations (7)
1