Loss of alpha-globin genes in human subjects is associated with improved nitric oxide-mediated vascular perfusion

Alpha thalassemia is a hemoglobinopathy on account of decreased manufacturing of the α-globin protein from loss of as much as 4 α-globin genes, with one or two lacking in the trait phenotype. Individuals with sickle cell illness who co-inherit the loss of one or two α-globin genes have been recognized…

MIR197

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NUP155

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RAB22A

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COL7A1

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EIF2B5

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FBXW10

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LYPD6B

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ACTL6A

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