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. 2020 May 11;12:63. doi: 10.1186/s13148-020-00856-y

Fig. 1.

Fig. 1

Sequencing results of the family with the donor splice site variant in intron 1 of the KCNQ1 gene. The patient and the patient’s mother carry the splice site variant in intron 1 of KCNQ1 (NM_000218.2(KCNQ1):c.386+1G>T). The patient is diagnosed with BWS due to IC2 LOM. The mother and the brother of the patient are healthy