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

Fig. 3.

Download original image
Fig. 3.

Sanger sequencing of the proband and her mother showing a missense variation (c.922A>G) resulting in a p.N308D mutation of the PTPN11 gene.

Journal of Genetic Medicine 2019;16:81-4 https://doi.org/10.5734/JGM.2019.16.2.81
© 2019 Korean Society of Medical Genetics and Genomics