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- W2943668286 abstract "Sickle cell disease (SCD) is an autosomal recessive disorder caused by a point mutation in the β globin gene that substitutes glutamic acid (GAG) at position 6 of the protein into valine (GTG).[1][1] The resulting mutated hemoglobin (HbS) polymerizes under hypoxic conditions driving sickling of red" @default.
- W2943668286 created "2019-05-09" @default.
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- W2943668286 date "2019-04-30" @default.
- W2943668286 modified "2023-10-18" @default.
- W2943668286 title "Factor H: a novel modulator in sickle cell disease" @default.
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- W2943668286 doi "https://doi.org/10.3324/haematol.2018.214668" @default.
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