bioRxiv / medRxiv
open access
Preclinical Basal Ganglia Neurodegeneration in Female X Linked Dystonia Parkinsonism Carriers
Background and ObjectivesX-linked dystonia-parkinsonism (XDP) is a severe neurodegenerative movement disorder caused by a retrotransposon insertion with a polymorphic hexanucleotide repeat expansion in the TAF1 gene. While the disease predominantly affects males, female carriers may exhibit a variab
Conceptio Open Archive
Analyze & explore related research in Conceptio
Connect this record directly into your research workflow or AI agent. Explore citations across open repositories, query full text, and export structured proof bundles.
This document is indexed with metadata only: full text is not available in the archive for this record. Open the official source ↗
Related documents
- Two insular regions are differentially involved in behavioral variant FTD and nonfluent/agrammatic variant PPA#1249972
- Surgery of Dystonia#889051
- The location of the t(4;14) translocation breakpoint within the NSD2 gene identifies a subset of patients with high-risk NDMM#121829
- Huntington's Disease and Huntington's Disease-like 2 (HDL2) in Martinique#235114
- Carrier frequency of autosomal recessive monogenic disorders in the peruvian population.#433906
Record · ID 1336121
Retrieved via Conceptio: every document is proof-bundled with source, license, and retrieval metadata.
Retrieved via Conceptio: every document is proof-bundled with source, license, and retrieval metadata.
Bring this data into your agent: Connect via MCP or API · 20 free credits to start · no card required
Read the Docs → · View CLI source on GitHub · Conceptio Open Knowledge Archive
Read the Docs → · View CLI source on GitHub · Conceptio Open Knowledge Archive