Your browser doesn't support javascript.
loading
Sub-cellular level resolution of common genetic variation in the photoreceptor layer identifies continuum between rare disease and common variation.
Currant, Hannah; Fitzgerald, Tomas W; Patel, Praveen J; Khawaja, Anthony P; Webster, Andrew R; Mahroo, Omar A; Birney, Ewan.
Affiliation
  • Currant H; European Molecular Biology Laboratory, European Bioinformatics Institute, Cambridge, United Kingdom.
  • Fitzgerald TW; Novo Nordisk Foundation Center for Protein Research, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
  • Patel PJ; European Molecular Biology Laboratory, European Bioinformatics Institute, Cambridge, United Kingdom.
  • Khawaja AP; NIHR Biomedical Research Centre, Moorfields Eye Hospital NHS Foundation Trust and UCL Institute of Ophthalmology, London, United Kingdom.
  • Mahroo OA; NIHR Biomedical Research Centre, Moorfields Eye Hospital NHS Foundation Trust and UCL Institute of Ophthalmology, London, United Kingdom.
  • Birney E; NIHR Biomedical Research Centre, Moorfields Eye Hospital NHS Foundation Trust and UCL Institute of Ophthalmology, London, United Kingdom.
PLoS Genet ; 19(2): e1010587, 2023 02.
Article in En | MEDLINE | ID: mdl-36848389
Subject(s)
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Rare Diseases / Genome-Wide Association Study Limits: Humans Language: En Journal: PLoS Genet Journal subject: GENETICA Year: 2023 Document type: Article Affiliation country: Reino Unido
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Rare Diseases / Genome-Wide Association Study Limits: Humans Language: En Journal: PLoS Genet Journal subject: GENETICA Year: 2023 Document type: Article Affiliation country: Reino Unido