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©The Author(s) 2022.
World J Clin Pediatr. Sep 9, 2022; 11(5): 429-436
Published online Sep 9, 2022. doi: 10.5409/wjcp.v11.i5.429
Published online Sep 9, 2022. doi: 10.5409/wjcp.v11.i5.429
Figure 2 Direct DNA sequence analysis of the ITGB2 gene.
A and B: Homozygous c.920T>C (p.Leu307Pro) mutation in exon 8 and homozygous c.758G>A (p.Arg253His) mutation in exon 7 in the genomic DNA of Patient 1; C and D: Heterozygous c.920T>C mutation in exon 8 and heterozygous c.758G>A mutation in exon 7 of both parents in Patient 1; E: homozygous c.262C>T (p.Gln88Ter) mutation in exon 4 in the genomic DNA of Patient 2; F: heterozygous c.262C>T mutation in both paternal and maternal DNA.
- Citation: Suksawat Y, Pacharn P, Siripipattanamongkol N, Boonyawat B. Three novel homozygous ITGB2 mutations among two patients with leukocyte adhesion defect type-1: Two case reports. World J Clin Pediatr 2022; 11(5): 429-436
- URL: https://www.wjgnet.com/2219-2808/full/v11/i5/429.htm
- DOI: https://dx.doi.org/10.5409/wjcp.v11.i5.429