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Galactosemia Diagnosis by Whole Exome Sequencing Later in Life.
Lucas-Del-Pozo, Sara; Moreno-Martinez, David; Camprodon-Gomez, Maria; Moreno-Martinez, Daniel; Hernández-Vara, Jorge.
Afiliação
  • Lucas-Del-Pozo S; Neurodegenerative Diseases Research Group Vall Hebron Research Institute, Vall Hebron University Hospital Barcelona Spain.
  • Moreno-Martinez D; Department of Clinical and Movement Neurosciences UCL Queen Square Institute of Neurology London United Kingdom.
  • Camprodon-Gomez M; Rare Diseases and Inborn Errors of Metabolism in Adult Unit Vall Hebron University Hospital Barcelona Spain.
  • Moreno-Martinez D; Lysosomal Storage Disorders Unit The Royal Free Hospital NHS Foundation Trust and University College London London United Kingdom.
  • Hernández-Vara J; Rare Diseases and Inborn Errors of Metabolism in Adult Unit Vall Hebron University Hospital Barcelona Spain.
Mov Disord Clin Pract ; 8(Suppl 1): S37-S39, 2021 Aug.
Article em En | MEDLINE | ID: mdl-34514046
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies Idioma: En Revista: Mov Disord Clin Pract Ano de publicação: 2021 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies Idioma: En Revista: Mov Disord Clin Pract Ano de publicação: 2021 Tipo de documento: Article