A novel double nucleotide variant in the ferritin‐L iron‐responsive element in a Finnish patient with hereditary hyperferritinaemia‐cataract syndrome

Publisher: John Wiley & Sons Inc

E-ISSN: 1755-3768|96|1|95-99

ISSN: 1755-375X

Source: ACTA OPHTHALMOLOGICA, Vol.96, Iss.1, 2018-02, pp. : 95-99

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Abstract