Isolated Paroxysmal Non-kinesigenic Dystonia Associated with Homozygous PDHB Variant in an Indian Family.

Agarwal, Pankaj A; Kuipers, Demy J S; Fevga, Christina; Agrawal, Shruti; Ravat, Sangeeta H; Breedveld, Guido J; Sethi, Kapil; Bonifati, Vincenzo

Agarwal, Pankaj A; Kuipers, Demy J S; Fevga, Christina; Agrawal, Shruti; Ravat, Sangeeta H; Breedveld, Guido J; Sethi, Kapil; Bonifati, Vincenzo.

Afiliação

Agarwal PA; Movement Disorders Clinic, Department of Neurology, Global Hospitals, Mumbai, India.
Kuipers DJS; Department of Neurology, Global Hospitals, Mumbai, India.
Fevga C; Department of Neurology, Seth GS Medical College and KEM Hospital, Mumbai, India.
Agrawal S; Department of Clinical Genetics, Erasmus MC, University Medical Center Rotterdam, Rotterdam, the Netherlands.
Ravat SH; Department of Clinical Genetics, Erasmus MC, University Medical Center Rotterdam, Rotterdam, the Netherlands.
Breedveld GJ; Department of Neurology, Seth GS Medical College and KEM Hospital, Mumbai, India.
Sethi K; Department of Neurology, Global Hospitals, Mumbai, India.
Bonifati V; Department of Neurology, Seth GS Medical College and KEM Hospital, Mumbai, India.

Mov Disord ; 37(10): 2166-2167, 2022 10.

Article em En | MEDLINE | ID: mdl-35838632

Assuntos

Distonia; Povo Asiático; Distonia/complicações; Distonia/genética; Homozigoto; Humanos; Proteínas do Tecido Nervoso/genética

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Distonia Tipo de estudo: Risk_factors_studies Limite: Humans Idioma: En Revista: Mov Disord Ano de publicação: 2022 Tipo de documento: Article

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