| 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 |
