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

I. Perrault; J. Halbritter; J. Porath; X. Gerard; D. Braun; H. Gee; H. Fathy; S. Saunier; V. Cormier-Daire; S. Thomas; T. Attié-Bitach; N. Boddaert; M. Taschner; M. Schueler; E. Lorentzen; R. Lifton; E. Otto; P. Bastin; J. Kaplan; F. Hildebrandt; J. M. Rozet

doi:10.1186/2046-2530-4-S1-P7

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

I. Perrault^*
, J. Halbritter
, J. Porath
, X. Gerard
, D. Braun
, H. Gee
, H. Fathy
, S. Saunier
, V. Cormier-Daire
, S. Thomas
, T. Attié-Bitach
, N. Boddaert
, M. Taschner
, M. Schueler
, E. Lorentzen
, R. Lifton
, E. Otto
, P. Bastin
, J. Kaplan
, F. Hildebrandt

J. M. Rozet

^*Corresponding author for this work

Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaper › Journal article › Research › peer-review

Original language	English
Article number	P7
Journal	Cilia
Issue	SUPPLEMENT 1
DOIs	https://doi.org/10.1186/2046-2530-4-S1-P7
Publication status	Published - 13 Jul 2015
Externally published	Yes

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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., ... Rozet, J. M. (2015). Mutations of IFT81, encoding an IFT-B core protein, as a rare cause of a ciliopathy. Cilia, (SUPPLEMENT 1), Article P7. https://doi.org/10.1186/2046-2530-4-S1-P7

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

author = "I. Perrault and J. Halbritter and J. Porath and X. Gerard and D. Braun and H. Gee and H. Fathy and S. Saunier and V. Cormier-Daire and S. Thomas and T. Atti{\'e}-Bitach and N. Boddaert and M. Taschner and M. Schueler and E. Lorentzen and R. Lifton and E. Otto and P. Bastin and J. Kaplan and F. Hildebrandt and Rozet, \{J. M.\}",

year = "2015",

month = jul,

day = "13",

doi = "10.1186/2046-2530-4-S1-P7",

language = "English",

journal = "Cilia",

number = "SUPPLEMENT 1",

}

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 2015, 'Mutations of IFT81, encoding an IFT-B core protein, as a rare cause of a ciliopathy', Cilia, no. SUPPLEMENT 1, P7. https://doi.org/10.1186/2046-2530-4-S1-P7

TY - JOUR

T1 - Mutations of IFT81, encoding an IFT-B core protein, as a rare cause of a ciliopathy

AU - Perrault, I.

AU - Halbritter, J.

AU - Porath, J.

AU - Gerard, X.

AU - Braun, D.

AU - Gee, H.

AU - Fathy, H.

AU - Saunier, S.

AU - Cormier-Daire, V.

AU - Thomas, S.

AU - Attié-Bitach, T.

AU - Boddaert, N.

AU - Taschner, M.

AU - Schueler, M.

AU - Lorentzen, E.

AU - Lifton, R.

AU - Otto, E.

AU - Bastin, P.

AU - Kaplan, J.

AU - Hildebrandt, F.

AU - Rozet, J. M.

PY - 2015/7/13

Y1 - 2015/7/13

UR - https://www.scopus.com/pages/publications/84999633631

U2 - 10.1186/2046-2530-4-S1-P7

DO - 10.1186/2046-2530-4-S1-P7

M3 - Journal article

AN - SCOPUS:84999633631

JO - Cilia

JF - Cilia

IS - SUPPLEMENT 1

M1 - P7

ER -

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

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