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Author/Creator Perrault, I

2. Abnormal respiratory cilia in non-syndromic Leber congenital amaurosis with CEP290 mutations. Issue 12 (30th August 2010)

Authors:
Papon, J F; Perrault, I; Coste, A; Louis, B; Gérard, X; Hanein, S; Fares-Taie, L; Gerber, S; Defoort-Dhellemmes, S; Vojtek, A M; Kaplan, J; Rozet, J M; Escudier, E
Journal:
Journal of medical genetics
Issue:
Volume 47:Issue 12(2010)
Page Start:
829
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

6. Mutations of IFT81, encoding an IFT-B core protein, as a rare cause of a ciliopathy. Issue 1 (December 2015)

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
Journal:
Cilia
Issue:
Volume 4:Issue 1(2015)
Page Start:
1
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗