The <i>SLC40A1</i> R178Q mutation is a recurrent cause of hemochromatosis and is associated with a novel pathogenic mechanism

Chandran Ka, Julie Guellec, Xavier Pepermans, Caroline Kannengiesser, Cécile Ged, Wim Wuyts, David Cassiman, Victor de Ledinghen, Bruno Varet, Caroline de Kerguenec, Claire Oudin, Isabelle Gourlaouen, Thibaud Lefebvre, Claude Férec, Isabelle Callebaut, Gérald Le Gac

Open source

DOI: 10.3324/haematol.2018.189845
Published: 2018-07-12
Container: Haematologica
Publisher: Ferrata Storti Foundation (Haematologica)
Open access: unknown

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Cite this work

BibTeX

@article{allodium:10.3324/haematol.2018.189845,
  title = {The
                    <i>SLC40A1</i>
                    R178Q mutation is a recurrent cause of hemochromatosis and is associated with a novel pathogenic mechanism},
  author = {Chandran Ka and Julie Guellec and Xavier Pepermans and Caroline Kannengiesser and Cécile Ged and Wim Wuyts and David Cassiman and Victor de Ledinghen and Bruno Varet and Caroline de Kerguenec and Claire Oudin and Isabelle Gourlaouen and Thibaud Lefebvre and Claude Férec and Isabelle Callebaut and Gérald Le Gac},
  year = {2018},
  journal = {Haematologica},
  doi = {10.3324/haematol.2018.189845},
  url = {https://doi.org/10.3324/haematol.2018.189845}
}

RIS

TY  - JOUR
TI  - The
                    <i>SLC40A1</i>
                    R178Q mutation is a recurrent cause of hemochromatosis and is associated with a novel pathogenic mechanism
AU  - Chandran Ka
AU  - Julie Guellec
AU  - Xavier Pepermans
AU  - Caroline Kannengiesser
AU  - Cécile Ged
AU  - Wim Wuyts
AU  - David Cassiman
AU  - Victor de Ledinghen
AU  - Bruno Varet
AU  - Caroline de Kerguenec
AU  - Claire Oudin
AU  - Isabelle Gourlaouen
AU  - Thibaud Lefebvre
AU  - Claude Férec
AU  - Isabelle Callebaut
AU  - Gérald Le Gac
PY  - 2018
JO  - Haematologica
DO  - 10.3324/haematol.2018.189845
UR  - https://doi.org/10.3324/haematol.2018.189845
ER  -

APA

Ka, C., Guellec, J., Pepermans, X., Kannengiesser, C., Ged, C., Wuyts, W., Cassiman, D., Ledinghen, V. D., Varet, B., Kerguenec, C. D., Oudin, C., Gourlaouen, I., Lefebvre, T., Férec, C., Callebaut, I., & Gac, G. L. (2018). The <i>SLC40A1</i> R178Q mutation is a recurrent cause of hemochromatosis and is associated with a novel pathogenic mechanism. Haematologica. https://doi.org/10.3324/haematol.2018.189845

Source records

crossref · retrieved 2026-11-10T20:39:55.890Z