Abstract:
:We describe a case of beta-thalassemia (thal) trait in which the patient also carries a novel delta chain variant due to a missense mutation at amino acid codon 13 (GCC-->GAC, Ala-->Asp). The level of Hb A2 was not elevated, raising the potential for misdiagnosis.
journal_name
Hemoglobinjournal_title
Hemoglobinauthors
Walker L,Patterson M,Eng B,McFarlane A,Waye JSdoi
10.1080/03630260500310794keywords:
subject
Has Abstractpub_date
2005-01-01 00:00:00pages
285-7issue
4eissn
0363-0269issn
1532-432Xjournal_volume
29pub_type
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