描述
DNA sequencing chromatogram confirming the G114V (glycine to valine) mutation at codon 114 of the PRNP gene in affected family members, establishing the genetic basis of this hereditary prion disease.
Figure 3
DiagramSource Paper
Human prion disease with a G114V mutation and epidemiological studies in a Chinese family: a case series.Cite This Figure
 > Source: Jing Ye et al. "Human prion disease with a G114V mutation and epidemiological studies in a Chine." *Journal of medical case reports*, 2008. PMID: [18925969](https://pubmed.ncbi.nlm.nih.gov/18925969/)
<figure> <img src="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2576332/bin/1752-1947-2-331-3.jpg" alt="DNA sequencing chromatogram confirming the G114V (glycine to valine) mutation at codon 114 of the PRNP gene in affected family members, establishing the genetic basis of this hereditary prion disease." /> <figcaption>Figure 3. DNA sequencing chromatogram confirming the G114V (glycine to valine) mutation at codon 114 of the PRNP gene in affected family members, establishing the genetic basis of this hereditary prion disease.<br> Source: Jing Ye et al. "Human prion disease with a G114V mutation and epidemiological studies in a Chine." <em>Journal of medical case reports</em>, 2008. PMID: <a href="https://pubmed.ncbi.nlm.nih.gov/18925969/">18925969</a></figcaption> </figure>