Coinheritance of alleles associated with hemochromatosis and hereditary hyperferritinemia-cataract syndrome [2]

Blood

Volumn 92, Issue 11, 1998, Pages 4480-

  Barton, J C ^a   Beutler, E ^a   Gelbart, T ^a  

^a SOUTHERN IRON DISORDERS CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

FERRITIN;

ADULT; ALLELE; CASE REPORT; CATARACT; FEMALE; GENE MUTATION; GENETIC DISORDER; HEMOCHROMATOSIS; HUMAN; IRON METABOLISM; LETTER; PRIORITY JOURNAL; SYNDROME DELINEATION;

EID: 0032403421     PISSN: 00064971     EISSN: None     Source Type: Journal    
DOI: 10.1182/blood.v92.11.4480.423a57b_4480_4481     Document Type: Letter

References (10)