Description of a new mutation in the L-ferritin iron-responsive element associated with hereditary hyperferritinemia-cataract syndrome in a Spanish family [2]

Blood

Volumn 93, Issue 11, 1999, Pages 4020-4021

  Balas, A ^a   Aviles, M J ^a   Garcia Sanchez, F ^a   Vicario, J L ^a   Cervera, A ^a  

^a Regional Transfusion Centre   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

DNA FRAGMENT; FERRITIN;

CLINICAL FEATURE; DNA CONFORMATION; FAMILY STUDY; GENE MUTATION; GENETIC ASSOCIATION; HUMAN; HYPERFERRITINEMIA; IRON RESPONSIVE ELEMENT; LETTER; NUCLEIC ACID BASE SUBSTITUTION; NUCLEOTIDE SEQUENCE; PEDIGREE; PRIORITY JOURNAL; SEQUENCE ANALYSIS;

EID: 0033151541     PISSN: 00064971     EISSN: None     Source Type: Journal    
DOI: 10.1182/blood.v93.11.4020     Document Type: Letter

References (6)