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Article

PRKRA Mutation Causing Early-Onset Generalized Dystonia-Parkinsonism (DYT16) in an Italian Family.

Movement disorders : official journal of the Movement Disorder Society - 1 May 2016

Quadri Marialuisa, Olgiati Simone, Sensi Mariachiara, Gualandi Francesca, Groppo Elisabetta, Rispoli Vittorio, Graafland Josja, Breedveld Guido J, Fabbrini Giovanni, Berardelli Alfredo, Bonifati Vincenzo

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Identifiers

PMID: 26990861
DOI: 10.1002/mds.26583

Genes

PRKRA

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

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PRKRA Mutation Causing Early-Onset Generalized Dystonia-Parkinsonism (DYT16) in an Italian Family.PMID 26990861Read ↗

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DYT16: the original cases.Semantic proximity Read ↗

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Early onset primary dystonia.Semantic proximity Read ↗

DYT16, a novel young-onset dystonia-parkinsonism disorder: identification of a segregating mutation in the stress-response protein PRKRA.Semantic proximity Read ↗

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AOPEP variants as a novel cause of recessive dystonia: Generalized dystonia and dystonia-parkinsonism.Semantic proximity Read ↗

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Screening for THAP1 Mutations in Polish Patients with Dystonia Shows Known and Novel Substitutions.Semantic proximity Read ↗

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