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Case Reports
. 2021 Sep;100(9):2417-2419.
doi: 10.1007/s00277-020-04141-z. Epub 2020 Jun 17.

Type I congenital methemoglobinemia in a Chinese family

Affiliations
Case Reports

Type I congenital methemoglobinemia in a Chinese family

Jiang Ji et al. Ann Hematol. 2021 Sep.
No abstract available

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References

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    1. Curry S (1982) Methemoglobinemia. Ann Emerg Med 11(4):214–221. https://doi.org/10.1016/s0196-0644(82)80502-7 - DOI - PubMed
    1. Percy MJ, Lappin TR (2008) Recessive congenital methaemoglobinaemia: cytochrome b(5) reductase deficiency. Br J Haematol 141(3):298–308. https://doi.org/10.1111/j.1365-2141.2008.07017.x - DOI - PubMed
    1. Forestier A, Pissard S, Cretet J, Mambie A, Pascal L, Cliquennois M, Cambier N, Rose C (2015) Congenital recessive methemoglobinemia revealed in adulthood: description of a new mutation in cytochrome b5 reductase gene. Hemoglobin 39(6):438–441. https://doi.org/10.3109/03630269.2015.1065882 - DOI - PubMed
    1. Beutler E (2006) Williams Hematology. Methemoglobinemia and other causes of cyanosis, 7th edn. McGraw-Hill, New York

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