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The Interaction of Genetic Mutations in PARK2 and FA2H Causes a Novel Phenotype in a Case of Childhood-Onset Movement Disorder.
Benger, Matthew; Mankad, Kshitij; Proukakis, Christos; Mazarakis, Nicholas D; Kinali, Maria.
Afiliación
  • Benger M; Department of Neurosciences, King's College Hospital, London, United Kingdom.
  • Mankad K; Department of Neuroradiology, Great Ormond Street Hospital, London, United Kingdom.
  • Proukakis C; Institute of Neurology, University College London, London, United Kingdom.
  • Mazarakis ND; Centre for Neuroinflammation & Neurodegeneration, Imperial College, London, United Kingdom.
  • Kinali M; Honorary Senior Lecturer in Paediatric Neurology, Imperial College, London, United Kingdom.
Front Neurol ; 10: 555, 2019.
Article en En | MEDLINE | ID: mdl-31191442
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Etiology_studies / Prognostic_studies Idioma: En Revista: Front Neurol Año: 2019 Tipo del documento: Article País de afiliación: Reino Unido
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Etiology_studies / Prognostic_studies Idioma: En Revista: Front Neurol Año: 2019 Tipo del documento: Article País de afiliación: Reino Unido