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- W2005337064 abstract "We have recently studied a family with a rare combination of two abnormal α-globin genes. The combination of a two-base (AA) deletion in the α2 polyadenylation signal (poly A) (AATAAA→AATA– –) and a 3.7 kb α gene deletion, found in two children, resulted in a moderately severe thalassemic condition. Both parents and three siblings were tested and the hematological condition and molecular findings are presented. The father was born in India with Portuguese and British ancestry; the mother is of Dutch ancestry. All three siblings were born in Australia." @default.
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- W2005337064 date "2007-01-01" @default.
- W2005337064 modified "2023-10-11" @default.
- W2005337064 title "A Moderately Severe α-Thalassemia Condition Resulting From a Combination of the α2 Polyadenylation Signal (AATA<i>AA</i>→AATA– –) Mutation and a 3.7 Kb α Gene Deletion in an Australian Family" @default.
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- W2005337064 doi "https://doi.org/10.1080/03630260701288997" @default.
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