Copyright
©The Author(s) 2021.
World J Clin Cases. Jul 6, 2021; 9(19): 5245-5251
Published online Jul 6, 2021. doi: 10.12998/wjcc.v9.i19.5245
Published online Jul 6, 2021. doi: 10.12998/wjcc.v9.i19.5245
Figure 2 Genomic sequence of the patient.
Genetic analysis revealed a heterozygous null mutation in the patient’s ankyrin gene [c.841C > T (p. Arg281Ter)]. No genetic mutations were found in his parents. The arrows indicated the mutation site.
- Citation: Wang JF, Ma L, Gong XH, Cai C, Sun JJ. Severe hyperbilirubinemia in a neonate with hereditary spherocytosis due to a de novo ankyrin mutation: A case report. World J Clin Cases 2021; 9(19): 5245-5251
- URL: https://www.wjgnet.com/2307-8960/full/v9/i19/5245.htm
- DOI: https://dx.doi.org/10.12998/wjcc.v9.i19.5245