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. 2019 Oct 24;9(2):137–141. doi: 10.1055/s-0039-1700519

Fig. 3.

Fig. 3

Pedigree depicting the biological relationship and inheritance pattern of the genetic mutation c.178C > T of the NDUFA12 gene resulting in Leigh syndrome and the c.732_733delAA mutation of the GNPTAB gene, causing mucolipidosis II α/beta. The patient in the presented case is indicated by an arrow.