EPS6.06 A comprehensive catalog of variation in the CFTR gene von Raraigh, K.S., Petren, K.M., Rommens, J.M.

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P117 The variation in cystic fibrosis transmembrane conductance regulator variants in Canada and around the world von Cheng, S.Y., Abdulrahem, N., Eckford, P.D.W., Raraigh, K.S., Stephenson, A.L.

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WS13.1 Patients with mutations that permit 3% or more of wild-type CFTR function are associated with higher FEV1 von Sosnay, P.R, Raraigh, K.S, Vangoor, F, Yu, H, Penland, C.M, Corey, M, Lewis, M.H, Castellani, C, Rommens, J, Cutting, G.R

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WS17.3 Functional characterisation and CFTR2 disease liability assignment of 48 missense variants von Raraigh, K.S., Han, S., Davis, E., Evans, T., Pellicore, M., Mccague, A., Joynt, A., Lu, Z., Atalar, M., Sharma, N., Sosnay, P.R., Cutting, G.

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