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Fig. 3 | Journal of Medical Case Reports

Fig. 3

From: Clinical and molecular findings in a Moroccan family with Jervell and Lange-Nielsen syndrome: a case report

Fig. 3

Electropherograms of the identified c.1343dupC; p.Glu449Argfs*14 mutation. The proband IV:1 presented with the homozygous c.1343dupC; p.Glu449Argfs*14 mutation and both parents (III:5 and III:6) and unaffected brother IV:2 are heterozygotes. One healthy brother (IV:3) was homozygous for the wild-type allele. The X indicates the position of detected mutation (Duplication of C base). The arrows indicate the location of the mutated base

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Journal of Medical Case Reports

ISSN: 1752-1947