fig1

Detection of leukocyte adhesion deficiency type 1 in an infant by high-throughput targeted exome sequencing

Figure 1. A: The sequencing exposes a homozygous mutation c.817G>A (p.G273R) in ITGB2 gene in the proband; B: his father carries the mutation; C: his mother does not carry the mutation; D: normal is the control of QPCR for chr21:46320235-46320435, showing that the mother is normal

Journal of Translational Genetics and Genomics
ISSN 2578-5281 (Online)
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