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Hereditary Spherocytosis: Can Next-Generation Sequencing of the Five Most Frequently Affected Genes Replace Time-Consuming Functional Investigations?
Häuser, Friederike; Rossmann, Heidi; Adenaeuer, Anke; Shrestha, Annette; Marandiuc, Dana; Paret, Claudia; Faber, Jörg; Lackner, Karl J; Lämmle, Bernhard; Beck, Olaf.
Afiliación
  • Häuser F; Institute of Clinical Chemistry and Laboratory Medicine, University Medical Center of the Johannes Gutenberg University, 55131 Mainz, Germany.
  • Rossmann H; Institute of Clinical Chemistry and Laboratory Medicine, University Medical Center of the Johannes Gutenberg University, 55131 Mainz, Germany.
  • Adenaeuer A; Institute of Clinical Chemistry and Laboratory Medicine, University Medical Center of the Johannes Gutenberg University, 55131 Mainz, Germany.
  • Shrestha A; Institute of Clinical Chemistry and Laboratory Medicine, University Medical Center of the Johannes Gutenberg University, 55131 Mainz, Germany.
  • Marandiuc D; Transfusion Center, University Medical Center of the Johannes Gutenberg University, 55131 Mainz, Germany.
  • Paret C; Department of Pediatric Hematology, Oncology & Hemostaseology, Center for Pediatric and Adolescent Medicine, University Medical Center of the Johannes Gutenberg University, 55131 Mainz, Germany.
  • Faber J; Department of Pediatric Hematology, Oncology & Hemostaseology, Center for Pediatric and Adolescent Medicine, University Medical Center of the Johannes Gutenberg University, 55131 Mainz, Germany.
  • Lackner KJ; Institute of Clinical Chemistry and Laboratory Medicine, University Medical Center of the Johannes Gutenberg University, 55131 Mainz, Germany.
  • Lämmle B; Center for Thrombosis and Hemostasis (CTH), University Medical Center of the Johannes Gutenberg University, 55131 Mainz, Germany.
  • Beck O; Department of Hematology and Central Hematology Laboratory, Inselspital, Bern University Hospital, University of Bern, 3010 Bern, Switzerland.
Int J Mol Sci ; 24(23)2023 Nov 30.
Article en En | MEDLINE | ID: mdl-38069343
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Esferocitosis Hereditaria / Ancirinas Límite: Child / Humans Idioma: En Revista: Int J Mol Sci Año: 2023 Tipo del documento: Article País de afiliación: Alemania Pais de publicación: Suiza
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Esferocitosis Hereditaria / Ancirinas Límite: Child / Humans Idioma: En Revista: Int J Mol Sci Año: 2023 Tipo del documento: Article País de afiliación: Alemania Pais de publicación: Suiza