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

Fig. 1.

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Fig. 1.

Pedigree and Sanger sequencing of SLC25A15 in the hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome patient. (A) Pedigree showing consanguineous parents and affected patients with HHH syndrome. (B) Partial Sanger sequencing of SLC25A15 showing homozygous mutations for G220R. Each mutation was inherited from her father and mother.

Journal of Genetic Medicine 2019;16:85-9 https://doi.org/10.5734/JGM.2019.16.2.85
© 2019 Korean Society of Medical Genetics and Genomics