Review articles | |
Hematology. 2021;26:896-903 | Ferritin L-subunit gene mutation and hereditary hyperferritinaemia cataract syndrome (HHCS): a case report and literature review |
Clin Chem Lab Med. 2019;57:1837-1845 | Hereditary hyperferritinaemia-cataract syndrome (HHCS) – an underestimated condition: ferritin light chain variant spectrum in German families |
Clinical practice guidelines | |
None available | |
Online evidence-based resources | |
DynaMed | A rigorous evidence-based point-of-care tool, can access overview and recommendations section without subscription |
UpToDate | Relies heavily on expert opinion. Not accessible without subscription |