Skip to main content
Egyptian Journal of Medical Human Genetics
Fig. 3 | Egyptian Journal of Medical Human Genetics

Fig. 3

From: The homozygous pathogenic variant of the POMGNT1 gene identified using whole-exome sequencing in Iranian family with congenital hydrocephalus

Fig. 3

Nuclear family’s sequencing chromatographs and agarose gel electrophoresis. Sanger sequencing demonstrated that both parents were carriers of the c.74 G>A variant in the POMGNT1 gene and confirmed the homozygous G>A alteration in the proband. Abbreviations: A: Adenine; G: Guanine; C: Cytosine; T: Thymine; L: Ladder; P: Proband; F: Father; M: Mother; and NTC: No-Template Control

Back to article page