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Mitochondrial DNA variants in genomic data: diagnostic uplifts and predictive implications.
Macken, William L; Lucassen, Anneke M; Hanna, Michael G; Pitceathly, Robert D S.
Affiliation
  • Macken WL; Department of Neuromuscular Diseases, UCL Queen Square Institute of Neurology and The National Hospital for Neurology and Neurosurgery, London, UK.
  • Lucassen AM; Wessex Clinical Genetics Service, Princess Anne Hospital, Southampton, UK.
  • Hanna MG; Wessex Clinical Genetics Service, Princess Anne Hospital, Southampton, UK.
  • Pitceathly RDS; Clinical Ethics and Law Group (CELS), Faculty of Medicine, University of Southampton, Southampton, UK.
Nat Rev Genet ; 22(9): 547-548, 2021 09.
Article in En | MEDLINE | ID: mdl-34050335
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: DNA, Mitochondrial / Genomics / Mitochondrial Diseases / Molecular Diagnostic Techniques / Whole Genome Sequencing / Mutation Type of study: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Limits: Humans Language: En Journal: Nat Rev Genet Journal subject: GENETICA Year: 2021 Document type: Article Affiliation country: Country of publication:
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: DNA, Mitochondrial / Genomics / Mitochondrial Diseases / Molecular Diagnostic Techniques / Whole Genome Sequencing / Mutation Type of study: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Limits: Humans Language: En Journal: Nat Rev Genet Journal subject: GENETICA Year: 2021 Document type: Article Affiliation country: Country of publication: