Sequence analysis of exon 1 of the ferritin light chain (FTL) gene can reveal the rare disorder ‘hereditary hyperferritinaemia without cataracts’

Research output: Contribution to journalArticle (Academic Journal)peer-review

3 Citations (Scopus)
263 Downloads (Pure)

Abstract

[no abstract]
Original languageEnglish
JournalBritish Journal of Haematology
Early online date23 May 2018
DOIs
Publication statusE-pub ahead of print - 23 May 2018

Keywords

  • iron overload
  • haemochromatosis
  • genetics

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