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A common variant in combination with a nonsense mutation in a member of the thioredoxin family causes primary ciliary dyskinesia

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https://hal-upec-upem.archives-ouvertes.fr/hal-00621951
Contributor : Jean-François Bercher <>
Submitted on : Sunday, September 11, 2011 - 4:23:06 PM
Last modification on : Wednesday, February 26, 2020 - 7:06:05 PM

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  • HAL Id : hal-00621951, version 1

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B. Duriez, P. Duquesnoy, E. Escudier, A.M. Bridoux, D. Escalier, et al.. A common variant in combination with a nonsense mutation in a member of the thioredoxin family causes primary ciliary dyskinesia. Proceedings of the National Academy of Sciences of the United States of America , National Academy of Sciences, 2007, 104 (9), pp.3336-3341. ⟨hal-00621951⟩

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