Article
Rare Pathogenic Variants in Pooled Whole-Exome Sequencing Data Suggest Hyperammonemia as a Possible Cause of Dementia Not Classified as Alzheimer's Disease or Frontotemporal Dementia.
Genes - 7 Jun 2024
Karachanak-Yankova Sena, Serbezov Dimitar, Antov Georgi, Stancheva Mikaela, Mihaylova Marta, Hadjidekova Savina, Toncheva Draga, Pashov Anastas, Belejanska Diyana, Zhelev Yavor, Petrova Mariya, Mehrabian Shima, Traykov Latchezar
Abstract excerpt
The genetic bases of Alzheimer's disease (AD) and frontotemporal dementia (FTD) have been comprehensively studied, which is not the case for atypical cases not classified into these diagnoses. In the present study, we aim to contribute to the molecular understanding of the development of non-AD and non-FTD dementia due to hyperammonemia caused by mutations in urea cycle genes. The analysis was performed by pooled...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
