Published in
BMJ Publishing Group, Journal of Medical Genetics, 10(52), p. 657-665, 2015
DOI: 10.1136/jmedgenet-2014-102838
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- [europepmc.org] | PDF
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IFT81, encoding an IFT-B core protein, as a very rare cause of a ciliopathy phenotype
Journal article published in 2015 by
Isabelle Perrault,
Jan Halbritter 
,
Jonathan D. Porath,
Xavier Gérard,
Daniela A. Braun,
Yung Heon,
Heon Yung Gee,
Hanan M. Fathy,
Sophie Saunier,
Valérie Cormier-Daire ,
Sophie Thomas,
Tania Attié-Bitach,
Nathalie Boddaert,
Michael Taschner,
Markus Schueler
and other authors.
,
Jonathan D. Porath,
Xavier Gérard,
Daniela A. Braun,
Yung Heon,
Heon Yung Gee,
Hanan M. Fathy,
Sophie Saunier,
Valérie Cormier-Daire ,
Sophie Thomas,
Tania Attié-Bitach,
Nathalie Boddaert,
Michael Taschner,
Markus Schueler
and other authors.
This paper is available in a repository.
Full text: Download
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