A novel deletion in the FTL gene causes hereditary hyperferritinemia cataract syndrome (HHCS) by alteration of the transcription start site. Journal Articles Refereed uri icon

Overview

Published in

  • Human Mutation

Time

Date/time value

  • 2007

Identity

Digital Object Identifier (DOI)

  • 10.1002/humu.9501

Additional Document Info

Parent Title

  • Hum Mutat

Volume

  • 28

Issue

  • 7

Publisher

  • John Wiley & Sons