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Volumn 130, Issue 9, 2000, Pages 324-328

Hereditary hyperferritinaemia cataract syndrome: Does it exist in Switzerland?

Author keywords

Cataract; Hyperferritinaemia; Iron metabolism

Indexed keywords

FERRITIN;

EID: 0034603356     PISSN: 00367672     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Conference Paper
Times cited : (10)

References (14)
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  • 2
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  • 4
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  • 5
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    • Cazzola, M.1    Bergamaschi, G.2    Tonon, L.3    Arbustini, E.4    Grasso, M.5    Vercesi, E.6
  • 6
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    • Girelli D, Corrocher R, Bisceglia L, Olivieri O, Zelante L, Panozzo G, et al. Hereditary hyperferritinemia cataract syndrome caused by a 29-base pair deletion in the iron-responsive element of ferritin L-subunit gene. Blood 1997;90: 2084-8.
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  • 7
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    • Girelli D, Corrocher R, Bisceglia L, Olivieri O, De Franceschi L, Zelante 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.
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  • 10
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  • 11
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  • 13
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.