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  • 1-3 ل  3 نتائج ل ""Apoferritins""

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Publication : ophthalmic genetics
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Academic Journal

Ferritin light chain gene mutation in a large Australian family with hereditary hyperferritinemia-cataract syndrome.

  • Authors : Yazar S; a Centre for Ophthalmology and Visual Science/Lions Eye Institute, University of Western Australia , Perth , Western Australia , Australia.; Franchina M

Subjects: Point Mutation*; Apoferritins/Apoferritins/Apoferritins/*genetics ; Cataract/Cataract/Cataract/*congenital Hyperferritinemia, hereditary, with congenital cataracts

  • Source: Ophthalmic genetics [Ophthalmic Genet] 2017 Mar-Apr; Vol. 38 (2), pp. 171-174. Date of Electronic Publication: 2016 Apr 20.Publisher: Informa Healthcare Country of Publication: England NLM ID: 9436057 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Hyperferritinemia-cataract syndrome: Long-term ophthalmic observations in an Italian family.

  • Authors : Cosentino I; a Medical Genetics, Molecular Medicine Department , Sapienza University , San Camillo-Forlanini Hospital, Rome , Italy.; Zeri F

Subjects: Cataract/Cataract/Cataract/*congenital ; Iron Metabolism Disorders/Iron Metabolism Disorders/Iron Metabolism Disorders/*congenital; Adult Hyperferritinemia, hereditary, with congenital cataracts

  • Source: Ophthalmic genetics [Ophthalmic Genet] 2016 Sep; Vol. 37 (3), pp. 318-22. Date of Electronic Publication: 2016 Feb 05.Publisher: Informa Healthcare Country of Publication: England NLM ID: 9436057 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Hyperferritinemia-cataract syndrome: Long-term ophthalmic observations in an Italian family

Subjects: 0301 basic medicine; Adult; Male

  • Source: Ophthalmic genetics. 37(3)

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  • 1-3 ل  3 نتائج ل ""Apoferritins""