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Matches in SemOpenAlex for { <https://semopenalex.org/work/W2463506112> ?p ?o ?g. }

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• W2463506112 abstract "Key Points Mutations in HSPA9 cause CSAs that may be inherited in a recessive or pseudodominant manner. HSPA9 loss-of-function alleles are often inherited in trans with a common coding single nucleotide polymorphism associated with altered gene expression." @default.
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• W2463506112 date "2015-12-17" @default.
• W2463506112 modified "2023-10-16" @default.
• W2463506112 title "Congenital sideroblastic anemia due to mutations in the mitochondrial HSP70 homologue HSPA9" @default.
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• W2463506112 doi "https://doi.org/10.1182/blood-2015-09-659854" @default.
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