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Defects in the IFT-B component IFT172 cause Jeune and Mainzer-Saldino syndromes in humans
Leo, PJ,
Gee, HY,
Tory, K,
Moorani, KN,
Leroux, MR,
Schmidts, M,
Porath, JD,
Hartley, JL,
Davis, EE,
Brown, MA,
Filhol, E,
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Tuysuz, B,
Schueler, M,
Kaplan, BS,
Scambler, PJ,
Czarnecki, PG,
Nitschké, P,
Shah, JV,
Halbritter, J,
Gardiner, B,
Bole-Feysot, C,
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Zhan, SH,
Li, C,
Krug, P,
Bizet, AA,
Constantinescu, A,
Jones, SJ,
Trnka, P,
Lehman, AM,
Braun, DA,
Krantz, ID,
Maher, ER,
Zankl, A,
McInerney-Leo, AM,
Knebelmann, B,
Kayserili, H
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Am. J. Hum. Genet. |
2013 |
23990561 |
Molecular basis of tubulin transport within the cilium by IFT74 and IFT81
Weber, K,
Mizuno, N,
Fort, C,
Bhogaraju, S,
Blisnick, T,
Nigg, EA,
Lamla, S,
Bastin, P,
Taschner, M,
Lorentzen, E,
Cajanek, L
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Science |
2013 |