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Sequence analysis of exon 1 of the ferritin light chain ( FTL ) gene can reveal the rare disorder ‘hereditary hyperferritinaemia without cataracts’
Author(s) -
Bhuva Meha,
Sen Sambit,
Elsey Terence,
Atoyebi Wale,
Dreau Helene,
Bradbury Charlotte,
Johnston Rosalynd,
Bignell Patricia,
Griffiths William
Publication year - 2019
Publication title -
british journal of haematology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.907
H-Index - 186
eISSN - 1365-2141
pISSN - 0007-1048
DOI - 10.1111/bjh.15231
Subject(s) - cataracts , exon , biology , genetics , ferritin , mutation , hemochromatosis , ferroportin , transferrin saturation , gene , medicine , pathology , serum ferritin , iron homeostasis