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An Indian Young-onset Dementia With Parkinsonism With Double Heterozygous Mutations in ABCA7 and PRKN Identified Through Whole-exome Sequencing.
Sadhukhan, Dipanwita; Mallick, Aishwarya; Mishra, Smriti; Mukherjee, Adreesh; Biswas, Atanu; Hui, Subhra P; Biswas, Arindam.
Afiliação
  • Sadhukhan D; Molecular Biology & Clinical Neuroscience Division, National Neurosciences Centre, Calcutta, Kolkata, India.
  • Mallick A; Molecular Biology & Clinical Neuroscience Division, National Neurosciences Centre, Calcutta, Kolkata, India.
  • Mishra S; Molecular Biology & Clinical Neuroscience Division, National Neurosciences Centre, Calcutta, Kolkata, India.
  • Mukherjee A; Bangur Institute of Neurosciences, IPGME&R, Kolkata, India.
  • Biswas A; Bangur Institute of Neurosciences, IPGME&R, Kolkata, India.
  • Hui SP; S. N. Pradhan Centre for Neurosciences, University of Calcutta, Kolkata, India.
  • Biswas A; Molecular Biology & Clinical Neuroscience Division, National Neurosciences Centre, Calcutta, Kolkata, India.
Alzheimer Dis Assoc Disord ; 37(2): 164-167, 2023.
Article em En | MEDLINE | ID: mdl-37253124
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doença de Parkinson / Transtornos Parkinsonianos / Demência / Doença de Alzheimer Idioma: En Ano de publicação: 2023 Tipo de documento: Article
Texto completo
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doença de Parkinson / Transtornos Parkinsonianos / Demência / Doença de Alzheimer Idioma: En Ano de publicação: 2023 Tipo de documento: Article