Search Results - "SERET, H"

Association of a nonsense mutation (W1282X), the most common mutation in the Ashkenazi Jewish cystic fibrosis patients in Israel, with presentation of severe disease by Shoshani, T, Augarten, A, Gazit, E, Bashan, N, Yahav, Y, Rivlin, Y, Tal, A, Seret, H, Yaar, L, Kerem, E

“…Only about 30% of the cystic fibrosis chromosomes in the Israeli cystic fibrosis patient populations carry the major CF mutation (delta F508). Since different…”
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Association of a nonsense mutation (W1282X), the most common mutation in the Ashkenazi Jewish cystic fibrosis patients in Israel, with presentiation of severe disease by SHOSHANI, T, AUGARTEN, A, KEREM, B.-S, GAZIT, E, BASHAN, N, YAHAV, Y, RIVLIN, Y, TAL, A, SERET, H, YAAR, L, KEREM, E

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