Homozygous PLA2G6 (PARK 14) gene mutation associated neuropsychiatric phenotypes from southern India.

Sakhardande, Kasturi Atmaram; Reddi, Venkata Senthil Kumar; Mishra, Shree; Navin, Karthick; Ramu, Aashraya; Arunachal, Gautham; Mangalore, Sandhya; Yadav, Ravi; Jain, Sanjeev

Sakhardande, Kasturi Atmaram; Reddi, Venkata Senthil Kumar; Mishra, Shree; Navin, Karthick; Ramu, Aashraya; Arunachal, Gautham; Mangalore, Sandhya; Yadav, Ravi; Jain, Sanjeev.

Afiliação

Sakhardande KA; Department of Psychiatry; National Institute of Mental Health and Neuro Sciences, Bangalore, India.
Reddi VSK; Department of Psychiatry; National Institute of Mental Health and Neuro Sciences, Bangalore, India. Electronic address: sreddi@nimhans.ac.in.
Mishra S; Department of Psychiatry; National Institute of Mental Health and Neuro Sciences, Bangalore, India.
Navin K; Department of Psychiatry; National Institute of Mental Health and Neuro Sciences, Bangalore, India.
Ramu A; Department of Psychiatry; National Institute of Mental Health and Neuro Sciences, Bangalore, India.
Arunachal G; Department of Human Genetics, National Institute of Mental Health and Neuro Sciences, Bangalore, India.
Mangalore S; Department of Neuroimaging and Intervention Radiology, National Institute of Mental Health and Neuro Sciences, Bangalore, India.
Yadav R; Department of Neurology;National Institute of Mental Health and Neuro Sciences, Bangalore, India.
Jain S; Department of Psychiatry; National Institute of Mental Health and Neuro Sciences, Bangalore, India.

Parkinsonism Relat Disord ; 90: 49-51, 2021 09.

Article em En | MEDLINE | ID: mdl-34365112

Assuntos

Fosfolipases A2 do Grupo VI/genética; Transtornos Heredodegenerativos do Sistema Nervoso/genética; População Branca/genética; Alelos; Variação Biológica da População; Feminino; Transtornos Heredodegenerativos do Sistema Nervoso/etnologia; Homozigoto; Humanos; Índia; Masculino; Ilustração Médica; Mutação; Fenótipo; Sequenciamento do Exoma; Adulto Jovem

Palavras-chave

Neuropsychiatric; PLA2G6; Parkinson's disease; Southern India

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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transtornos Heredodegenerativos do Sistema Nervoso / População Branca / Fosfolipases A2 do Grupo VI Tipo de estudo: Prognostic_studies / Qualitative_research / Risk_factors_studies Limite: Adult / Female / Humans / Male País como assunto: Asia Idioma: En Ano de publicação: 2021 Tipo de documento: Article

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