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GγAγ(β+) hereditary persistence of fetal hemoglobin: The Gγ – 158 C → T mutation in cis to the − 175 T → C mutation of the Aγ-globin gene results in increased Gγ-globin synthesis

✍ Scribed by M. B. Coleman; J. G. Adams III; M. H. Steinberg; M. W. Plonczynski; A. H. Harrell; O. Castro; W. P. Winter

Publisher: John Wiley and Sons
Year: 1993
Tongue: English
Weight: 483 KB
Volume: 42
Category: Article
ISSN: 0361-8609
DOI: 10.1002/ajh.2830420209

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