B. Cogn?


AuthID: R-00J-T3P

Publicações a aguardar confirmação

1
TÍTULO: Mutations in the Kinesin-2 Motor KIF3B Cause an Autosomal-Dominant Ciliopathy
AUTORES: Cogné, B; Latypova, X; Senaratne, LDS; Martin, L; Koboldt, DC; Kellaris, G; Fievet, L; Le Meur, G; Caldari, D; Debray, D; Nizon, M; Frengen, E; Bowne, SJ; Buckley, RM; Aberdein, D; Paulo Célio Alves ; Barsh, GS; Bellone, RR; Bergström, TF; Boyko, AR; Brockman, JA; Casal, ML; Castelhano, MG; Distl, O; Dodman, NH; Ellinwood, NM; Fogle, JE; Forman, OP; Garrick, DJ; Ginns, EI; Häggström, J; Harvey, RJ; Hasegawa, D; Haase, B; Helps, CR; Hernandez, I; Hytönen, MK; Kaukonen, M; Kaelin, CB; Kosho, T; Leclerc, E; Lear, TL; Leeb, T; Li, RHL; Lohi, H; Longeri, M; Magnuson, MA; Malik, R; Mane, SP; Munday, JS; Murphy, WJ; Pedersen, NC; Rothschild, MF; Rusbridge, C; Shapiro, B; Stern, JA; Swanson, WF; Terio, KA; Todhunter, RJ; Warren, WC; Wilcox, EA; Wildschutte, JH; Yu, Y; Cadena, EL; Daiger, SP; Bujakowska, KM; Pierce, EA; Gorin, M; Katsanis, N; Bézieau, S; Petersen Jones, SM; Occelli, LM; Lyons, LA; Legeai Mallet, L; Sullivan, LS; Davis, EE; Isidor, B; ...Mais
PUBLICAÇÃO: 2020, FONTE: American Journal of Human Genetics, VOLUME: 106, NÚMERO: 6
INDEXADO EM: Scopus CrossRef: 30

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