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- W4290802227 abstract "Abstract X-linked dystonia-parkinsonism (XDP) is a neurodegenerative movement disorder that primarily affects adult Filipino men. It is caused by a founder retrotransposon insertion in TAF1 that contains a hexanucleotide repeat, the number of which differs among the patients and correlates with the age at disease onset (AAO) and other clinical parameters. A recent work has identified additional genetic modifiers of age-associated penetrance in XDP, bringing to light the DNA mismatch repair genes MSH3 and PMS2 . Despite X-linked recessive inheritance, a minor subset of patients are female, manifesting the disease via various mechanisms such as homozygosity, imbalanced X-chromosome inactivation, or aneuploidy. Here, we summarize and discuss clinical and genetic aspects of XDP, with a focus on variable disease expressivity as a consequence of subtle genetic differences within a seemingly homogenous population of patients." @default.
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- W4290802227 date "2022-06-01" @default.
- W4290802227 modified "2023-09-25" @default.
- W4290802227 title "Factors influencing reduced penetrance and variable expressivity in X-linked dystonia-parkinsonism" @default.
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- W4290802227 doi "https://doi.org/10.1515/medgen-2022-2135" @default.
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