Contract grant sponsors: DHOS (general french healthcare management organization); INSERM; French Reference Centre for Rare Iron Overload Diseases of Genetic Origin.
Ferroportin Diseases: Functional Studies, a Link Between Genetic and Clinical Phenotype
Version of Record online: 11 SEP 2013
© 2013 WILEY PERIODICALS, INC.
Volume 34, Issue 11, pages 1529–1536, November 2013
How to Cite
Détivaud, L., Island, M.-L., Jouanolle, A.-M., Ropert, M., Bardou-Jacquet, E., Le Lan, C., Mosser, A., Leroyer, P., Deugnier, Y., David, V., Brissot, P. and Loréal, O. (2013), Ferroportin Diseases: Functional Studies, a Link Between Genetic and Clinical Phenotype. Hum. Mutat., 34: 1529–1536. doi: 10.1002/humu.22396
Communicated by Michel Goossens
- Issue online: 9 OCT 2013
- Version of Record online: 11 SEP 2013
- Accepted manuscript online: 13 AUG 2013 06:58AM EST
- Manuscript Accepted: 5 AUG 2013
- Manuscript Received: 4 APR 2013
- DHOS (general french healthcare management organization)
- French Reference Centre for Rare Iron Overload Diseases of Genetic Origin
Disclaimer: Supplementary materials have been peer-reviewed but not copyedited.
|humu22396-sup-0001-TableS1.pdf||178K||Supp. Table S1. Sequences of primers used to generate mutated FPN-GFP expression vectors|
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