High HFE mutation incidence in idiopathic erythrocytosis.

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Title: High HFE mutation incidence in idiopathic erythrocytosis.
Authors: Burlet B; Service d'Hématologie Biologique, Pôle Biologie, CHU de Dijon, Dijon, France., Bourgeois V; Service d'Hématologie Biologique, Pôle Biologie, CHU de Dijon, Dijon, France., Buriller C; Laboratoire de génétique chromosomique et moléculaire, Pôle Biologie, CHU de Dijon, Dijon, France., Aral B; Laboratoire de génétique chromosomique et moléculaire, Pôle Biologie, CHU de Dijon, Dijon, France., Airaud F; Service de Génétique Médicale, CHU de Nantes, Nantes, France., Garrec C; Service de Génétique Médicale, CHU de Nantes, Nantes, France., Bézieau S; Service de Génétique Médicale, CHU de Nantes, Nantes, France.; L'institut du Thorax, INSERM, CNRS, UNIV Nantes, Nantes, France., Gardie B; L'institut du Thorax, INSERM, CNRS, UNIV Nantes, Nantes, France.; Ecole Pratique des Hautes, EPHE, PSL research University, France.; Laboratory of Excellence GR-Ex, Paris., Girodon F; Service d'Hématologie Biologique, Pôle Biologie, CHU de Dijon, Dijon, France.; Laboratory of Excellence GR-Ex, Paris.; Inserm U1231, Université de Bourgogne, Dijon, France.
Source: British journal of haematology [Br J Haematol] 2019 May; Vol. 185 (4), pp. 794-795. Date of Electronic Publication: 2018 Nov 08.
Publication Type: Letter; Research Support, Non-U.S. Gov't; Comment
Journal Info: Publisher: Wiley-Blackwell Country of Publication: England NLM ID: 0372544 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1365-2141 (Electronic) Linking ISSN: 00071048 NLM ISO Abbreviation: Br J Haematol Subsets: MEDLINE
Database: MEDLINE Ultimate
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  Data: High HFE mutation incidence in idiopathic erythrocytosis.
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  Data: <searchLink fieldCode="AU" term="%22Burlet+B%22">Burlet B</searchLink>; Service d'Hématologie Biologique, Pôle Biologie, CHU de Dijon, Dijon, France.<br /><searchLink fieldCode="AU" term="%22Bourgeois+V%22">Bourgeois V</searchLink>; Service d'Hématologie Biologique, Pôle Biologie, CHU de Dijon, Dijon, France.<br /><searchLink fieldCode="AU" term="%22Buriller+C%22">Buriller C</searchLink>; Laboratoire de génétique chromosomique et moléculaire, Pôle Biologie, CHU de Dijon, Dijon, France.<br /><searchLink fieldCode="AU" term="%22Aral+B%22">Aral B</searchLink>; Laboratoire de génétique chromosomique et moléculaire, Pôle Biologie, CHU de Dijon, Dijon, France.<br /><searchLink fieldCode="AU" term="%22Airaud+F%22">Airaud F</searchLink>; Service de Génétique Médicale, CHU de Nantes, Nantes, France.<br /><searchLink fieldCode="AU" term="%22Garrec+C%22">Garrec C</searchLink>; Service de Génétique Médicale, CHU de Nantes, Nantes, France.<br /><searchLink fieldCode="AU" term="%22Bézieau+S%22">Bézieau S</searchLink>; Service de Génétique Médicale, CHU de Nantes, Nantes, France.; L'institut du Thorax, INSERM, CNRS, UNIV Nantes, Nantes, France.<br /><searchLink fieldCode="AU" term="%22Gardie+B%22">Gardie B</searchLink>; L'institut du Thorax, INSERM, CNRS, UNIV Nantes, Nantes, France.; Ecole Pratique des Hautes, EPHE, PSL research University, France.; Laboratory of Excellence GR-Ex, Paris.<br /><searchLink fieldCode="AU" term="%22Girodon+F%22">Girodon F</searchLink>; Service d'Hématologie Biologique, Pôle Biologie, CHU de Dijon, Dijon, France.; Laboratory of Excellence GR-Ex, Paris.; Inserm U1231, Université de Bourgogne, Dijon, France.
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  Data: Letter; Research Support, Non-U.S. Gov't; Comment
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