Adaptive Modelling of Mutated FMO3 Enzyme Could Unveil Unexplored Scenarios Linking Variant Haplotypes to TMAU Phenotypes

Background: Trimethylaminuria (TMAU) is a rare genetic disease characterized by the accumulation of trimethylamine (TMA) and its subsequent excretion trough main body fluids, determining the characteristic fish odour in affected patients. We realized an experimental study to investigate the role of...

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Detalles Bibliográficos
Autores principales: Alibrandi, Simona, Nicita, Fabiana, Donato, Luigi, Scimone, Concetta, Rinaldi, Carmela, D’Angelo, Rosalia, Sidoti, Antonina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8618768/
https://www.ncbi.nlm.nih.gov/pubmed/34834137
http://dx.doi.org/10.3390/molecules26227045

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8618768/
https://www.ncbi.nlm.nih.gov/pubmed/34834137
http://dx.doi.org/10.3390/molecules26227045

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