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Fig. 1 | BMC Medical Genomics

Fig. 1

From: Next-generation sequencing for identifying a novel/de novo pathogenic variant in a Mexican patient with cystic fibrosis: a case report

Fig. 1

a Family pedigree showing the carriers of variants c.3266G > A, p.Trp1089* and c.1762G > T, p.Glu588*, and the patient with both variants (p.Trp1089*/p.Glu588*). b Sanger sequencing of the patient, father, and mother. Left, sequence of the variant c.3266G > A, p.Trp1089*. Right, sequence of the variant c.1762G > T, p.Glu588*

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