Clinicogenetic Characterization of Patients with PD and Heterozygous GBA1 Variants in an Indian Cohort.

Kamath, Sneha D; Holla, Vikram V; Phulpagar, Prashant; Kamble, Nitish; Yadav, Ravi; Muthusamy, Babylakshmi; Pal, Pramod Kumar

Kamath, Sneha D; Holla, Vikram V; Phulpagar, Prashant; Kamble, Nitish; Yadav, Ravi; Muthusamy, Babylakshmi; Pal, Pramod Kumar.

Afiliação

Kamath SD; Department of Neurology, National Institute of Mental Health and Neurosciences, Bengaluru, India.
Holla VV; Department of Neurology, National Institute of Mental Health and Neurosciences, Bengaluru, India.
Phulpagar P; Institute of Bioinformatics, International Technology Park, Bengaluru, India.
Kamble N; Manipal Academy of Higher Education, Manipal, India.
Yadav R; Department of Neurology, National Institute of Mental Health and Neurosciences, Bengaluru, India.
Muthusamy B; Department of Neurology, National Institute of Mental Health and Neurosciences, Bengaluru, India.
Pal PK; Institute of Bioinformatics, International Technology Park, Bengaluru, India.

Mov Disord ; 39(3): 628-630, 2024 Mar.

Article em En | MEDLINE | ID: mdl-38124431

Assuntos

Doença de Parkinson; Humanos; Glucosilceramidase/genética; Mutação/genética

Palavras-chave

GBA1; Parkinson disease; exome sequencing

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Parkinson Limite: Humans Idioma: En Revista: Mov Disord Assunto da revista: NEUROLOGIA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Índia

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