Search Results - "Saied, Zacharia"

A Tunisian patient with CLCN2‐related leukoencephalopathy by Ben Mohamed, Dina, Saied, Zacharia, Ben Sassi, Samia, Ben Said, Mariem, Nabli, Fatma, Achouri, Afef, Jeridi, Cyrine, Masmoudi, Saber, Amouri, Rim

“…CLCN2‐related leukoencephalopathy (CC2L OMIM#: 615651) is a recently identified rare disorder. It is caused by autosomal recessive mutations in the CLCN2 gene…”
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Genetic heterogeneity within a consanguineous family involving TTPA and SETX genes by Jeridi, Cyrine, Rachdi, Amine, Nabli, Fatma, Saied, Zacharia, Zouari, Rania, Ben Mohamed, Dina, Ben Said, Mariem, Masmoudi, Saber, Ben Sassi, Samia, Amouri, Rim

“…Autosomal recessive cerebellar ataxias (ARCA) constitute a highly heterogeneous group of progressive neurodegenerative disorders that typically occur prior to…”
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