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About this Biochemistry, Genetics and Molecular Biology article

Autosomal recessive IFT57 hypomorphic mutation cause ciliary transport defect in unclassified oral-facial-digital syndrome with short stature and brachymesophalangia by Thevenon, J.; Duplomb, L.; Phadke, S.; Eguether, T.; Saunier, A.; Avila, M.; Carmignac, V.; Bruel, A.-L.; St-Onge, J.; Duffourd, Y.; Pazour, G.J.; Franco, B.; Attie-Bitach, T.; Masurel-Paulet, A.; Rivière, J.-B.; Cormier-Daire, V.; Philippe, C.; Faivre, L.; Thauvin-Robinet, C. is a Biochemistry, Genetics and Molecular Biology article available to read on EtoBox.

It is typically read by researchers, students, and practitioners in Biochemistry, Genetics and Molecular Biology.

Author
Thevenon, J.; Duplomb, L.; Phadke, S.; Eguether, T.; Saunier, A.; Avila, M.; Carmignac, V.; Bruel, A.-L.; St-Onge, J.; Duffourd, Y.; Pazour, G.J.; Franco, B.; Attie-Bitach, T.; Masurel-Paulet, A.; Rivière, J.-B.; Cormier-Daire, V.; Philippe, C.; Faivre, L.; Thauvin-Robinet, C.
Publisher
John Wiley and Sons; Wiley (Blackwell Publishing); Blackwell Publishing Inc.; Wiley (ISSN 0009-9163)
Published
2016
Language
EN
Field
Biochemistry, Genetics and Molecular Biology (Life Sciences)

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