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Search Results - Bejrachandra, Sasithorn
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Mutations in Krüppel-like factor 1 cause transfusion-dependent hemolytic anemia and persistence of embryonic globin gene expression
by
Viprakasit, Vip
,
Ekwattanakit, Supachai
,
Riolueang, Suchada
,
Chalaow, Nipon
,
Fisher, Chris
,
Lower, Karen
,
Kanno, Hitoshi
,
Tachavanich, Kalaya
,
Bejrachandra, Sasithorn
,
Saipin, Jariya
,
Juntharaniyom, Monthana
,
Sanpakit, Kleebsabai
,
Tanphaichitr, Voravarn S.
,
Songdej, Duantida
,
Babbs, Christian
,
Gibbons, Richard J.
,
Philipsen, Sjaak
,
Higgs, Douglas R.
Published in
Blood
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Blood
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Adolescent
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Adult
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Alpha-Globins - Metabolism
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Amino Acid Sequence
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Anemia, Hemolytic - Blood
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Anemia, Hemolytic - Etiology
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Anemia, Hemolytic - Genetics
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Beta-Globins - Metabolism
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Child
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Child, Preschool
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Conserved Sequence
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Erythrocyte Indices
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Erythrocytes - Metabolism
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Female
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Fetal Hemoglobin - Chemistry
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Fetal Hemoglobin - Genetics
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Gene Expression Regulation
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Gene Order
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