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808 : Sequence analysis of exon 1 of the ferritin light chain (FTL) gene can reveal the rare but benign diagnosis of ‘hereditary hyperferriti‐ naemia without cataracts’

Researchers

Presenter

  • Meha Bhuva

Principal Investigators

  • Sambit Sen

  • Patel Jay

  • Rosalynd Johnston

  • Charlotte Bradbury

  • Terence Elsey

  • Wale Atoyebi

  • Patricia Bignell

  • William Griffiths

Medical Centers

  • Gastroenterology and Hepatology, Luton and Dunstable Hospital, London, United Kingdom

  • Brighton and Sussex University Hospitals NHS Trust, Sussex Cancer Centre, Brighton, United Kingdom

  • Haematology/BMT, University Hospitals Bristol, Bristol, United Kingdom

  • Molecular Genetics, Cambridge University Hospitals, Cambridge, United Kingdom

  • Translational Gastroenterology Unit, University of Oxford, Oxford, United Kingdom

  • Oxford Muscle and Nerve Centre, John Radcliffe Hospital, Oxford, United Kingdom

  • Cambridge University Hospitals, Cambridge, United Kingdom

Locations

  • United Kingdom

Companies

  • N/A

Study Components

Therapeutic Area

  • Ophthalmology (OP)

Disease

  • Cataract

Biomarkers

  • N/A

Drug/Treatment

  • N/A

Outcome

  • N/A

Study Design

  • N/A

Phase

  • NA

Study Id's

  • N/A

Sponsors

  • N/A

Result

  • N/A

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