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Microtubule dysfunction precedes transport impairment and mitochondria damage in MPP+-induced neurodegenerationCARTELLI, Daniele; RONCHI, Cristina; MAGGIONI, Maria G et al.Journal of neurochemistry. 2010, Vol 115, Num 1, pp 247-258, issn 0022-3042, 12 p.Article

High phenotypic intrafamilial variability in patients with Pendred syndrome and a novel duplication in the SLC26A4 gene : clinical characterization and functional studies of the mutated SLC26A4 proteinFUGAZZOLA, Laura; CIRELLO, Valentina; PAULMICHL, Markus et al.European journal of endocrinology. 2007, Vol 157, Num 3, pp 331-338, issn 0804-4643, 8 p.Article

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