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Rare coinheritance of hemoglobin vancleave with severe beta-thalassemia mutation in a patient with secondary erythrocytosis

IF 1 Q4 GENETICS & HEREDITY
Human Genome Variation Pub Date : 2024-04-23 DOI:10.1038/s41439-024-00275-y
Nur Aisyah Aziz, Nurul Hidayah Musa, Melina Mathews, Komalah Thevii Rajenderan, F. S. Abdul Hamid, S. Hassan, Syahira Lazira Omar, Wan Nurul Afiqha Binti Wan Yusoff, Melanie Ling Binti Mohd Din, Nurul Amira Jamaludin, W. R. Wan taib, E. Esa, Norafiza Mohd Yasin
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一名继发性红细胞增多症患者罕见的血红蛋白Vancleave与严重β地中海贫血突变共同遗传
本文章由计算机程序翻译，如有差异，请以英文原文为准。
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来源期刊
Human Genome Variation
Human Genome Variation Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
2.30
自引率
0.00%
发文量
39
审稿时长
13 weeks
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