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Article

Refinement of the DYT15 locus in myoclonus dystonia.

Movement disorders : official journal of the Movement Disorder Society - 30 Apr 2007

Han Fabin, Racacho Lemuel, Lang Anthony E, Bulman Dennis E, Grimes David A

Abstract excerpt

Inherited myoclonus dystonia (MD) is an autosomal dominant disorder in which we previously mapped a novel locus to chromosome18p11 (OMIM number: 607488). Since no further informative STS markers were found within the flanking shared regions, we utilized single nucleotide polymorphisms (SNP) for fine-mapping. All known or predicted genes within this region were directly sequenced. We identified three recombinant...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 17274032
DOI: 10.1002/mds.21400

Genes

STS

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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