Systematically testing human HMBS missense variants to reveal mechanism and pathogenic variation

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Defects in hydroxymethylbilane synthase (HMBS) can cause acute intermittent porphyria (AIP), an acute neurological disease. Although sequencing-based diagnosis can be definitive, ∼⅓ of clinical HMBS variants are missense variants, and most clinically reported HMBS missense variants are designated as...

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Detalles Bibliográficos
Autores principales: van Loggerenberg, Warren, Sowlati-Hashjin, Shahin, Weile, Jochen, Hamilton, Rayna, Chawla, Aditya, Sheykhkarimli, Dayag, Gebbia, Marinella, Kishore, Nishka, Frésard, Laure, Mustajoki, Sami, Pischik, Elena, Di Pierro, Elena, Barbaro, Michela, Floderus, Ylva, Schmitt, Caroline, Gouya, Laurent, Colavin, Alexandre, Nussbaum, Robert, Friesema, Edith C.H., Kauppinen, Raili, To-Figueras, Jordi, Aarsand, Aasne K., Desnick, Robert J., Garton, Michael, Roth, Frederick P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10577081/
https://www.ncbi.nlm.nih.gov/pubmed/37729906
http://dx.doi.org/10.1016/j.ajhg.2023.08.012

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10577081/
https://www.ncbi.nlm.nih.gov/pubmed/37729906
http://dx.doi.org/10.1016/j.ajhg.2023.08.012

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