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Mechanisms of Mitochondrial Dysfunction in Lysosomal Storage Disorders: A Review.
Stepien, Karolina M; Roncaroli, Federico; Turton, Nadia; Hendriksz, Christian J; Roberts, Mark; Heaton, Robert A; Hargreaves, Iain.
Afiliação
  • Stepien KM; Adult Inherited Metabolic Diseases, Salford Royal NHS Foundation Trust, Salford M6 8HD, UK.
  • Roncaroli F; Division of Neuroscience and Experimental Psychology, School of Biology, Medicine and Health, University of Manchester and Manchester Centre for Clinical Neuroscience, Salford Royal NHS Foundation Trust, Salford M6 8HD, UK.
  • Turton N; School of Pharmacy, Liverpool John Moore University, Byrom Street, Liverpool L3 3AF, UK.
  • Hendriksz CJ; Paediatrics and Child Health, Steve Biko Academic Unit, University of Pretoria, 0002 Pretoria, South Africa.
  • Roberts M; Neurology Department, Salford Royal NHS Foundation Trust, Salford M6 8HD, UK.
  • Heaton RA; School of Pharmacy, Liverpool John Moore University, Byrom Street, Liverpool L3 3AF, UK.
  • Hargreaves I; School of Pharmacy, Liverpool John Moore University, Byrom Street, Liverpool L3 3AF, UK.
J Clin Med ; 9(8)2020 Aug 11.
Article em En | MEDLINE | ID: mdl-32796538

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article