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Fig. 3 | BMC Medical Genetics

Fig. 3

From: Prenatal diagnosis of Duchenne muscular dystrophy revealed a novel mosaic mutation in Dystrophin gene: a case report

Fig. 3

Sanger analysis for the Dystrophin gene of the designated family members. a Overview of identified mutations. Note that c.6794delG mutant generated a truncated dystrophin protein (p.Gly2265Glu Efs × 6), while c.6796delA mutant resulted in a truncated dystrophin protein (p.Ile2266phe Efs × 5). b-f Confirmation of the mutations by Sanger sequencing from the proband (b), the mother (c, e), the sister of the proband (d), and the aunty of the proband (f). Reference sequence for Dystrophin gene: NM_004006.3

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