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Article

Movement disorders in 2016: from genes to phenotypes.

The Lancet. Neurology - 1 Jan 2017

Calabresi Paolo, Tambasco Nicola

Abstract excerpt

No abstract is available from the source.

Topics

Genetic Variation
Humans
Leucine-Rich Repeat Serine-Threonine Protein Kinase-2
Movement Disorders
Mutation
Phenotype

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 27979359
DOI: 10.1016/S1474-4422(16)30345-3

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 31 Aug 2026.

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