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

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Article dans une revue
Proceedings of the National Academy of Sciences of the United States of America , National Academy of Sciences, 2007, 104 (9), pp.3336-3341
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https://hal-upec-upem.archives-ouvertes.fr/hal-00621951
Contributeur : Jean-François Bercher <>
Soumis le : dimanche 11 septembre 2011 - 16:23:06
Dernière modification le : mercredi 15 avril 2015 - 16:11:52

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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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