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Filters: Author is Beck, Bodo B  [Clear All Filters]
2013
Gee HYung, Saisawat P, Ashraf S, Hurd TW, Vega-Warner V, Fang H, Beck BB, Gribouval O, Zhou W, Diaz KA et al..  2013.  ARHGDIA mutations cause nephrotic syndrome via defective RHO GTPase signaling.. J Clin Invest. 123(8):3243-53.