Mutations in AP2S1 cause familial hypocalciuric hypercalcemia type 3 - Nesbit, M A; Hannan, F; Howles, S A; Reed, A A; Cranston, T; Thakker, C E; Gregory, L; Rimmer, A J; Rust, N; Graham, U; Morrison, P J; Hunter, S J; Whyte, M P; McVean, G; Buck, D; Thakker, R V (Nat Genet, 2013)