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Liu XD, Yang K, Xiao J, Huang H, et al. Whole exome sequencing identifies a novel SPTB frameshift mutation causing
hereditary spherocytosis in the Chinese population. Ann Hematol 2022;101:2355-2357.
PMID: 35726106
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Liu XD, Yang K, Xiao J, Huang H, et al. Whole exome sequencing identifies a novel SPTB frameshift mutation causing
hereditary spherocytosis in the Chinese population. Ann Hematol 2022;101:2355-2357.
PMID: 35726106
|
|
|
|