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Novel mutations in <i>SPTA1<\/i> and <i>SPTB<\/i> identified by whole exome sequencing in eight Thai families with hereditary pyropoikilocytosis presenting with severe fetal and neonatal anaemia. Br J Haematol 185: 578-582, 2019.","DOI":"10.1111\/bjh.15559"},{"key":"5","doi-asserted-by":"crossref","unstructured":"5. Bogardus H, Schulz VP, Maksimova Y, et al. Severe nondominant hereditary spherocytosis due to uniparental isodisomy at the <i>SPTA1<\/i> locus. Haematologica 99: e168-e170, 2014.","DOI":"10.3324\/haematol.2014.110312"},{"key":"6","doi-asserted-by":"crossref","unstructured":"6. Chonat S, Risinger M, Sakthivel H, et al. The spectrum of <i>SPTA1<\/i>-associated hereditary spherocytosis. Front Physiol 10: 815, 2019.","DOI":"10.3389\/fphys.2019.01331"},{"key":"7","doi-asserted-by":"crossref","unstructured":"7. Wang X, Liu A, Lu Y, Hu Q. Novel compound heterozygous mutations in the <i>SPTA1<\/i> gene, causing hereditary spherocytosis in a neonate with Coombs-negative hemolytic jaundice. Mol Med Rep 19: 2801-2807, 2019.","DOI":"10.3892\/mmr.2019.9947"},{"key":"8","doi-asserted-by":"crossref","unstructured":"8. Xi Y, Wang L, Zhang P, Jia M, Li Z. A novel mutation in <i>SPTA1<\/i> identified by whole exome sequencing in a Chinese family for hereditary elliptocytosis presenting with hyperbilirubinemia: a case report. Medicine (Baltimore) 98: e15800, 2019.","DOI":"10.1097\/MD.0000000000015800"},{"key":"9","doi-asserted-by":"crossref","unstructured":"9. Wichterle H, Hanspal M, Palek J, Jarolim P. Combination of two mutant alpha spectrin alleles underlies a severe spherocytic hemolytic anemia. J Clin Invest 98: 2300-2307, 1996.","DOI":"10.1172\/JCI119041"},{"key":"10","doi-asserted-by":"crossref","unstructured":"10. Maruo Y, Nakahara S, Yanagi T, et al. Genotype of <i>UGT1A1<\/i> and phenotype correlation between Crigler-Najjar syndrome type II and Gilbert syndrome. J Gastroenterol Hepatol 31: 403-408, 2016.","DOI":"10.1111\/jgh.13071"},{"key":"11","doi-asserted-by":"crossref","unstructured":"11. Lee MJ, Chang YH, Kang SH, et al. A case of hereditary spherocytosis coexisting with Gilbert&apos;s syndrome. Korean J Gastroenterol 61: 166-169, 2013.","DOI":"10.4166\/kjg.2013.61.3.166"},{"key":"12","doi-asserted-by":"publisher","unstructured":"12. del Giudice EM, Perrotta S, Nobili B, Specchia C, d&apos;Urzo G, Iolascon A. Coinheritance of Gilbert syndrome increases the risk for developing gallstones in patients with hereditary spherocytosis. 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