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Fig. 2 | BMC Gastroenterology

Fig. 2

From: Clinical characteristics and STK11 gene mutations in Chinese children with Peutz-Jeghers syndrome

Fig. 2

STK11 gene sequencing results. a The variant (481het_dupA) in exon 4 of the STK11 gene in Case 1. b Mutation c.658C > C/T in exon 5 of Case 2. c Mutation c.943_944het_delCCinsG in exon 8 of Case 3. d The variant (c.397het_delG) in exon 3 of the STK11 gene in Case 4. e The variant (c.890G > G/A) in exon 7 of the STK11 gene in Case 5. f The variant (c.862 + 1G > G/A) in intron 6 of the STK11 gene in Case 6. g Case 7 carries a c.1062C > C/G mutation in exon 8. h Mutation c.290 + 1G > G/A in intron 1 of Case 8. i The variant (c.348_349het_delGT) in exon 2 of Case 9. j Case 11 carries a c.803_804het_delGGinsC mutation in exon 6. k Case 12 carries a c.121_139del19insTT mutation in exon 1. The red arrows indicate the mutation sites

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