Miscellaneous Iron-Related Disorders
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Publisher
Humana Press
Link
http://link.springer.com/content/pdf/10.1007/978-1-60327-485-2_21.pdf
Reference150 articles.
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4. Girelli D, Corrocher R, Bisceglia L, et al. Molecular basis for the recently described hereditary hyperferritinemia-cataract syndrome: a mutation in the iron-responsive element of ferritin L-subunit gene (the “Verona mutation”). Blood. 1995;86:4050–3.
5. Millonig G, Muckenthaler MU, Mueller S. Hyperferritinaemia-cataract syndrome: worldwide mutations and phenotype of an increasingly diagnosed genetic disorder. Hum Genomics. 2010;4:250–62.
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