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Volumn 100, Issue 2, 2002, Pages 695-697

Autosomal dominant reticuloendothelial iron overload associated with a 3-base pair deletion in the ferroportin 1 gene (SLC11A3)

Author keywords

[No Author keywords available]

Indexed keywords

CARRIER PROTEIN; FERROPORTIN 1; IRON; UNCLASSIFIED DRUG;

EID: 0037100382     PISSN: 00064971     EISSN: None     Source Type: Journal    
DOI: 10.1182/blood-2001-11-0132     Document Type: Article
Times cited : (161)

References (14)
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    • 0005600868 scopus 로고    scopus 로고
    • A simple genetic test identifies 90% of UK patients with haemochromatosis
    • (1997) Gut , vol.41 , pp. 841-844
  • 4
  • 12
    • 0032521230 scopus 로고    scopus 로고
    • Molecular modelling of ligand and mutation sites of the type A domains of human von Willebrand factor and their relevance to von Willebrand's disease
    • (1998) Blood , vol.91 , pp. 2032-2044
    • Jenkins, P.V.1    Pasi, K.J.2    Perkins, S.J.3
  • 13
    • 0036289142 scopus 로고    scopus 로고
    • Molecular modelling of mutations in the C-terminal domains of factor H of human complement: A new insight into haemolytic uraemic syndrome
    • (2002) J Mol Biol , vol.316 , pp. 217-224
    • Perkins, S.J.1    Goodship, T.H.J.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.