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Biallelic mutations in the SARS2 gene presenting as congenital sideroblastic anemia.
Colin, Elia; Courtois, Geneviève; Brouzes, Chantal; Pulman, Juliette; Rabant, Marion; Rötig, Agnès; Taffin, Hélène; Lion-Lambert, Mathilde; Fabrega, Sylvie; Da Costa, Lydie; De Montalembert, Mariane; Salomon, Rémi; Hermine, Olivier; Couronné, Lucile.
  • Colin E; Laboratory of cellular and molecular mechanisms of hematological disorders and therapeutic implications, INSERM U1163, Imagine Institute, University of Paris, Laboratory of Excellence GR-Ex, Paris. elia.colin@hotmail.fr.
  • Courtois G; Laboratory of cellular and molecular mechanisms of hematological disorders and therapeutic implications, INSERM U1163, Imagine Institute, University of Paris, Laboratory of Excellence GR-Ex, Paris.
  • Brouzes C; Hematology Laboratory, Hôpital Necker-Enfants Malades, Assistance publique-Hôpitaux de Paris (AP-HP), Paris.
  • Pulman J; Laboratory for Genetics of Mitochondrial Disorders, INSERM U1163, Imagine Institute, University of Paris, Paris.
  • Rabant M; Department of Pathology, Hôpital Necker - Enfants Malades, Assistance Publique-Hôpitaux de Paris, University of Paris, Paris.
  • Rötig A; Laboratory for Genetics of Mitochondrial Disorders, INSERM U1163, Imagine Institute, University of Paris, Paris.
  • Taffin H; Department of Pediatric Nephrology, MARHEA, Hôpital Necker - Enfants Malades, Assistance Publique-Hôpitaux de Paris (AP-HP), Paris.
  • Lion-Lambert M; Department of Pediatric Nephrology, MARHEA, Hôpital Necker - Enfants Malades, Assistance Publique-Hôpitaux de Paris (AP-HP), Paris.
  • Fabrega S; VVTG platform, SFR Necker, Paris.
  • Da Costa L; Hematology Laboratory, Robert Debré Hospital, Assistance Publique-Hôpitaux de Paris (AP-HP), Paris, France, University of Paris, Laboratory of Excellence GR-Ex, Paris.
  • De Montalembert M; Department of General Pediatrics and Pediatric Infectious Diseases, Reference Center for Sickle Cell Disease, Hôpital Necker - Enfants Malades, Assistance Publique-Hôpitaux de Paris (AP-HP), Université de Paris, Paris.
  • Salomon R; Department of Pediatric Nephrology, MARHEA, Hôpital Necker - Enfants Malades, Assistance Publique-Hôpitaux de Paris (AP-HP), Paris.
  • Hermine O; Hematology Department, Hôpital Necker - Enfants Malades, Assistance Publique - Hôpitaux de Paris (APHP), Laboratory of cellular and molecular mechanisms of hematological disorders and therapeutical Implications, INSERM U1163, Imagine Institute; University of Paris, Laboratory of Excellence GR-Ex, Pa
  • Couronné L; Laboratory of Onco-Hematology, Hôpital Necker - Enfants Malades, Assistance Publique - Hôpitaux de Paris (APHP), Laboratory of cellular and molecular mechanisms of hematological disorders and therapeutical Implications, INSERM U1163, Imagine Institute, University of Paris, Laboratory of Excellence G
Haematologica ; 106(12): 3202-3205, 2021 12 01.
Article in English | MEDLINE | ID: covidwho-1363591
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Genetic Diseases, X-Linked / COVID-19 / Anemia, Sideroblastic Type of study: Diagnostic study Limits: Humans Language: English Journal: Haematologica Year: 2021 Document Type: Article

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Genetic Diseases, X-Linked / COVID-19 / Anemia, Sideroblastic Type of study: Diagnostic study Limits: Humans Language: English Journal: Haematologica Year: 2021 Document Type: Article