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Explore mutations supported or not supported by publications registered in PubMed |
- Koenig SN, Cavus O, Williams J, Bernier M, Tonniges J, Sucharki H, Dew T, Akel M, Baker P, Madiai F, De Giorgi F, Scietti L, Faravelli S, Forneris F, Mohler PJ, Bradley EA (2021). "New Mechanistic Insights to PLOD1-mediated Human Vascular Disease." Transl Res (in press) - DOI - PubMed - Mutations
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SiMPLOD ID | Isoenzyme | Mutation | Disease phenotype | CLINVAR | Reference papers | Viewer |
---|---|---|---|---|---|---|
SiMPLOD1-178 | Lysyl Hydroxylase 1 (human) | LH1 SER178ARG (PLOD1 c.534C>A) |
Kyphoscoliotic Ehlers-Danlos Syndrome (Type VIa) Uncertain significance |
459821 | View |
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