References

Reference	Comment
*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

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