Mutations of IFT81, encoding an IFT-B core protein, as a rare cause of a ciliopathy

Shranjeno v:
Bibliografske podrobnosti
izdano v:Cilia
Main Authors: Perrault, I, Halbritter, J, Porath, J, Gerard, X, Braun, D, Gee, H, Fathy, H, Saunier, S, Cormier-Daire, V, Thomas, S, Attié-Bitach, T, Boddaert, N, Taschner, M, Schueler, M, Lorentzen, E, Lifton, R, Otto, E, Bastin, P, Kaplan, J, Hildebrandt, F, Rozet, JM
Format: Artigo
Jezik:Inglês
Izdano: BioMed Central 2015
Teme:
Poster Presentation
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC4519174/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/2046-2530-4-S1-P7
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