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Hereditary hyperferritinemia-cataract syndrome (HHCS) presenting with iron deficiency anemia associated with a new mutation in the iron responsive element of the L ferritin gene in a swiss family

✍ Scribed by Axel Rüfer; Jeremy P. Howell; Alex P. Lange; Raina Yamamoto; Julia Heuscher; Michael Gregor; Walter A. Wuillemin

No coin nor oath required. For personal study only.

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