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Autore Titolo [ Tipo] Anno Filtri: First Letter Of Title è C and Autore is Girotto, Giorgia [Clear All Filters]
Common variants in UMOD associate with urinary uromodulin levels: a meta-analysis. J Am Soc Nephrol 2014;25(8):1869-82.
. Consanguinity and hereditary hearing loss in Qatar. Hum Hered 2014;77(1-4):175-82.
. Cx26 partial loss causes accelerated presbycusis by redox imbalance and dysregulation of Nfr2 pathway. Redox Biol 2018;19:301-317.
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