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Article

Pallidonigroluysian atrophy associated with p.A152T variant in MAPT.

Parkinsonism & related disorders - 1 Sept 2013

Graff-Radford Jonathan, Whitwell Jennifer L, Dickson Dennis W, Josephs Keith A

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Share to Atrophy
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Share to Supranuclear Palsy, Progressive

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 23692670
DOI: 10.1016/j.parkreldis.2013.04.023

Genes

MAPT

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

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Pallidonigroluysian atrophy associated with p.A152T variant in MAPT.PMID 23692670Read ↗

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Functional MAPT haplotypes: Bridging the gap between genotype and neuropathologySemantic proximity Read ↗

MAPT H1 haplotype is a risk factor for essential tremor and multiple system atrophy.Semantic proximity Read ↗

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