Genetic analysis of acute intermittent porphyria caused by novel classical splicing variant in the insertion region of 29-residue specific to human HMBS protein

Background: Acute intermittent porphyria (AIP; OMIM#176000) is a genetic disorder that is caused by mutations in the hydroxymethylbilane synthetase (HMBS) gene. This gene encodes the third enzyme in the heme biosynthesis pathway. Human HMBS (hHMBS) contains a 29-residue insert (residues 296-324) at...

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Detalles Bibliográficos
Autores principales: Liang, Lei, Meng, Haixia, Wu, Haotian, Zhao, Jianrong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Molecular Biosciences
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10448817/
https://www.ncbi.nlm.nih.gov/pubmed/37635937
http://dx.doi.org/10.3389/fmolb.2023.1230798

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10448817/
https://www.ncbi.nlm.nih.gov/pubmed/37635937
http://dx.doi.org/10.3389/fmolb.2023.1230798

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