Your browser doesn't support javascript.
loading
Episodic ataxia in child with 16p11.2 deletion including PRRT2.
Padmanabha, Hansashree; Raghavendra, K; Arunachal, Gautham; Nagaraj, A R; Harishma, R S; Nashi, Saraswati; Pooja, M; Mathuranath, P S; Mahale, Rohan.
Afiliação
  • Padmanabha H; Department of Neurology, National Institute of Mental Health and Neurosciences (NIMHANS), Bangalore, 560029, India.
  • Raghavendra K; Department of Neurology, National Institute of Mental Health and Neurosciences (NIMHANS), Bangalore, 560029, India.
  • Arunachal G; Department of Human Genetics, National Institute of Mental Health and Neurosciences (NIMHANS), Bangalore, 560029, India.
  • Nagaraj AR; Department of Neurology, National Institute of Mental Health and Neurosciences (NIMHANS), Bangalore, 560029, India.
  • Harishma RS; Department of Neurology, National Institute of Mental Health and Neurosciences (NIMHANS), Bangalore, 560029, India.
  • Nashi S; Department of Neurology, National Institute of Mental Health and Neurosciences (NIMHANS), Bangalore, 560029, India.
  • Pooja M; Department of Neurology, National Institute of Mental Health and Neurosciences (NIMHANS), Bangalore, 560029, India.
  • Mathuranath PS; Department of Neurology, National Institute of Mental Health and Neurosciences (NIMHANS), Bangalore, 560029, India.
  • Mahale R; Department of Neurology, National Institute of Mental Health and Neurosciences (NIMHANS), Bangalore, 560029, India. Electronic address: rohanmahale83@gmail.com.
Parkinsonism Relat Disord ; 118: 105955, 2024 Jan.
Article em En | MEDLINE | ID: mdl-38091792
Assuntos
Palavras-chave
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ataxia / Deleção Cromossômica Limite: Child / Humans Idioma: En Revista: Parkinsonism Relat Disord Assunto da revista: NEUROLOGIA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Índia País de publicação: Reino Unido
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ataxia / Deleção Cromossômica Limite: Child / Humans Idioma: En Revista: Parkinsonism Relat Disord Assunto da revista: NEUROLOGIA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Índia País de publicação: Reino Unido