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

Volumn 86, Issue 11, 1995, Pages 4050-4053

  Girelli, D ^a   Corrocher, R ^a   Bisceglia, L ^a   Olivieri, O ^a   De Franceschi, L ^a   Zelante, L ^a   Gasparini, P ^a  

^a POLICLINICO BORGO ROMA   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; FERRITIN; IRON; RNA; TRANSFERRIN;

ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CHROMOSOMAL LOCALIZATION; CHROMOSOME 19Q; CLINICAL ARTICLE; CONGENITAL CATARACT; FERRITIN BLOOD LEVEL; GENE MUTATION; GENETIC DISORDER; HUMAN; HUMAN CELL; IRON DEFICIENCY ANEMIA; IRON RESPONSIVE ELEMENT; IRON STORAGE; PRIORITY JOURNAL; SINGLE STRAND CONFORMATION POLYMORPHISM; SYNDROME DELINEATION;

EID: 0028788201     PISSN: 00064971     EISSN: None     Source Type: Journal    
DOI: 10.1182/blood.v86.11.4050.bloodjournal86114050     Document Type: Article

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