Complex heterozygous mutations in hereditary spherocytosis: A case report

doi:10.12998/wjcc.v12.i18.3582

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Jun 26, 2024 (publication date) through Jul 17, 2024

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World Journal of Clinical Cases

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2307-8960

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Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA

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World J Clin Cases. Jun 26, 2024; 12(18): 3582-3588
Published online Jun 26, 2024. doi: 10.12998/wjcc.v12.i18.3582

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Figure 1 Sequencing results. A: ANK1 detected a new mutation from the patient's father; B: SPTA1 detected a new mutation from the patient's mother; C: The patient's sister ANK1 was not detected abnormal; D: Patient's sisters SPTA1 detected the genetic mutation of the mother.

Citation: He M, Lv YC, Wei YH, Liu LQ, Guo L, Li C. Complex heterozygous mutations in hereditary spherocytosis: A case report. World J Clin Cases 2024; 12(18): 3582-3588
URL: https://www.wjgnet.com/2307-8960/full/v12/i18/3582.htm
DOI: https://dx.doi.org/10.12998/wjcc.v12.i18.3582