Molecular basis for the hereditary hyperferritinemia-cataract syndrome [3]

Blood

Volumn 87, Issue 11, 1996, Pages 4912-4913

  Girelli, D ^a   Olivieri, O ^a   Gasparini, P ^a   Corrocher, R ^a  

^a UNIVERSITY OF VERONA   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID SUBSTITUTION; CATARACT; CHROMOSOME 19; GENE MUTATION; GENETIC DISORDER; HEMOSIDEROSIS; HUMAN; LETTER; PRIORITY JOURNAL; SITE DIRECTED MUTAGENESIS; SYNDROME;

EID: 0030011316     PISSN: 00064971     EISSN: None     Source Type: Journal    
DOI: 10.1182/blood.v87.11.4912.bloodjournal87114912     Document Type: Letter

References (0)