Journal of Genetic Medicine : eISSN 2383-8442 / pISSN 1226-1769

Fig. 1.

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Fig. 1.

Electropherogram of Sanger sequencing. The patient (A) and his mother (B) share the same heterozygous mutation on CAV3, while his father (C) and sister (D) do not have the mutation. The red arrows indicate the genomic position where the deletion starts.

Journal of Genetic Medicine 2019;16:67-70 https://doi.org/10.5734/JGM.2019.16.2.67
© 2019 Korean Society of Medical Genetics and Genomics