We present the first description of a Chinese family with a rare b-thalassemia mutation commonly observed in black Americans. This mutation is a splice donor site mutation, and is associated with a phenotype of beta0-thalassemia.
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Article Information
Vol. 90 No. 12 (2005): December, 2005 : Case Reports
Published
2005-01-01
Published By
Ferrata Storti Foundation, Pavia, Italy
Print ISSN
0390-6078
Online ISSN
1592-8721
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145
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71
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How to Cite
1.
C Liao, J Li, Y Huang, D Li. First detection of the splice donor site IVS-I-2 (T-->B) beta-thalassemia mutation in a Chinese patient. Haematologica 2005;90(12):1695-1695; https://doi.org/10.3324/%x.
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