Your browser doesn't support javascript.
loading
CPEO - Like mitochondrial myopathy associated with m.8340G>A mutation.
Tarnopolsky, Mark A; Sundaram, Arun N E; Provias, John; Brady, Lauren; Sadikovic, Bekim.
Affiliation
  • Tarnopolsky MA; Department of Pediatrics, McMaster University, Hamilton, Ontario, Canada. Electronic address: tarnopol@mcmaster.ca.
  • Sundaram ANE; Department of Ophthalmology and Vision Sciences, Sunnybrook Health Sciences Center, University of Toronto, Toronto, Ontario, Canada.
  • Provias J; Department of Pathology and Molecular Medicine, McMaster University, Hamilton, Ontario, Canada.
  • Brady L; Department of Pediatrics, McMaster University, Hamilton, Ontario, Canada.
  • Sadikovic B; Molecular Genetics Laboratory, Molecular Diagnostics Division, London Health Sciences Centre, Children's Health Research Institute, London, Ontario, Canada.
Mitochondrion ; 46: 69-72, 2019 05.
Article in En | MEDLINE | ID: mdl-29501485
Subject(s)
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: DNA, Mitochondrial / Point Mutation / Ophthalmoplegia, Chronic Progressive External Type of study: Risk_factors_studies Limits: Adult / Aged / Humans Language: En Journal: Mitochondrion Year: 2019 Document type: Article Country of publication: Netherlands
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: DNA, Mitochondrial / Point Mutation / Ophthalmoplegia, Chronic Progressive External Type of study: Risk_factors_studies Limits: Adult / Aged / Humans Language: En Journal: Mitochondrion Year: 2019 Document type: Article Country of publication: Netherlands