Export 3 results:
Autore Titolo Tipo [ Anno
Filtri: Autore è Girotto, Giorgia and First Letter Of Title is C [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.
.