The hereditary hyperferritinaemia-cataract syndrome;Hereditair hyperferritinemie-cataractsyndroom

Nederlands Tijdschrift voor Geneeskunde

Volumn 147, Issue 39, 2003, Pages 1923-1928

  Van der Klooster, J M ^a  

^a IKAZIA HOSPITAL   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

FERRITIN;

ADULT; AGED; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CASE REPORT; CATARACT EXTRACTION; CHROMOSOME 19; CLINICAL FEATURE; DIAGNOSTIC ACCURACY; DIFFERENTIAL DIAGNOSIS; DISEASE COURSE; DNA DETERMINATION; FEMALE; GENETIC COUNSELING; GENETIC VARIABILITY; HEMOCHROMATOSIS; HUMAN; HYPERFERRITINEMIA CATARACT SYNDROME; MALE; PATIENT COUNSELING; POINT MUTATION; PROTEIN BINDING; RNA TRANSLATION; TREATMENT OUTCOME; TREATMENT PLANNING;

ADULT; AGED; CATARACT; CHROMOSOMES, HUMAN, PAIR 19; DNA MUTATIONAL ANALYSIS; FEMALE; FERRITINS; HUMANS; LENS, CRYSTALLINE; MALE; PEDIGREE; POINT MUTATION; SYNDROME;

EID: 0141683704     PISSN: 00282162     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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