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Delineation of CCDC39/CCDC40 mutation spectrum and associated phenotypes in primary ciliary dyskines...

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Delineation of CCDC39/CCDC40 mutation spectrum and associated phenotypes in primary ciliary dyskines...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3555958

Delineation of CCDC39/CCDC40 mutation spectrum and associated phenotypes in primary ciliary dyskinesia

About this item

Full title

Delineation of CCDC39/CCDC40 mutation spectrum and associated phenotypes in primary ciliary dyskinesia

Author / Creator

Legendre, M , Blanchon, S , Copin, B , Duquesnoy, P , Montantin, G , Kott, E , Dastot, F , Jeanson, L , Cachanado, M , Rousseau, A , Papon, JF , Tamalet, A , Vojtek, AM , Escalier, D , Coste, A , de Blic, J , Clément, A , Escudier, E and Amselem, S

Publisher

BioMed Central Ltd

Journal title

Cilia (London), 2012-11, Vol.1 (S1), p.P91-P91, Article P91

Language

English

Formats

Articles

Publication information

Publisher

BioMed Central Ltd

Subjects

More information

Alternative Titles

Full title

Delineation of CCDC39/CCDC40 mutation spectrum and associated phenotypes in primary ciliary dyskinesia

Authors, Artists and Contributors

Author / Creator

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3555958

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3555958

Other Identifiers

ISSN

2046-2530

E-ISSN

2046-2530

DOI

10.1186/2046-2530-1-S1-P91

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