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Erschienen in: Annals of Hematology 1/2019

01.07.2018 | Letter to the Editor

Next-generation sequencing identified a novel SPTB frameshift insertion causing hereditary spherocytosis in China

verfasst von: Lan-Lan Meng, Shi-Min Yuan, Chao-Feng Tu, Ge Lin, Guang-Xiu Lu, Yue-Qiu Tan

Erschienen in: Annals of Hematology | Ausgabe 1/2019

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Dear editor, …
Literatur
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Zurück zum Zitat Del Orbe Barreto R, Arrizabalaga B, De la Hoz AB, Garcia-Orad A, Tejada MI, Garcia-Ruiz JC, Fidalgo T, Bento C, Manco L, Ribeiro ML (2016) Detection of new pathogenic mutations in patients with congenital haemolytic anaemia using next-generation sequencing. Int J Lab Hematol 38(6):629–638. https://doi.org/10.1111/ijlh.12551 CrossRefPubMed Del Orbe Barreto R, Arrizabalaga B, De la Hoz AB, Garcia-Orad A, Tejada MI, Garcia-Ruiz JC, Fidalgo T, Bento C, Manco L, Ribeiro ML (2016) Detection of new pathogenic mutations in patients with congenital haemolytic anaemia using next-generation sequencing. Int J Lab Hematol 38(6):629–638. https://​doi.​org/​10.​1111/​ijlh.​12551 CrossRefPubMed
Metadaten
Titel
Next-generation sequencing identified a novel SPTB frameshift insertion causing hereditary spherocytosis in China
verfasst von
Lan-Lan Meng
Shi-Min Yuan
Chao-Feng Tu
Ge Lin
Guang-Xiu Lu
Yue-Qiu Tan
Publikationsdatum
01.07.2018
Verlag
Springer Berlin Heidelberg
Erschienen in
Annals of Hematology / Ausgabe 1/2019
Print ISSN: 0939-5555
Elektronische ISSN: 1432-0584
DOI
https://doi.org/10.1007/s00277-018-3417-3

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