Molecular and clinical study of a cohort of 110 Algerian patients with autosomal recessive ataxia. Wahiba Hamza, Lamia Ali Pacha, Tarik Hamadouche, Jean Muller, Nathalie Drouot, Farida Ferrat, Samira Makri, Malika Chaouch, Meriem Tazir, Michel Koenig and Traki Benhassine; BMC Medical Genetics 2015, 16:36 doi:10.1186/s12881-015-0180-3
OPEN ACCESS, Full text Pdf
Subscribe to:
Posts (Atom)
