Novel human pathological mutations. Gene symbol: SLC40A1. Disease: haemochromatosis, type 4.

Human genetics

Volumn 125, Issue 3, 2009, Pages 338-

  Relvas, Luís ^a   Claro, Maria Teresa ^a   Bento, Maria Celeste ^a   Ribeiro, Maria Letícia ^a  

^a CENTRO HOSPITALAR E UNIVERSITÁRIO DE COIMBRA   (Portugal)

Author keywords

[No Author keywords available]

Indexed keywords

CATION TRANSPORT PROTEIN; FERRITIN; METAL TRANSPORTING PROTEIN 1; TRANSFERRIN;

AMINO ACID SUBSTITUTION; ARTICLE; BLOOD; CLASSIFICATION; CODON; FEMALE; GENETICS; HEMOCHROMATOSIS; HUMAN; IRON DEFICIENCY ANEMIA; METABOLISM; MISSENSE MUTATION; MOLECULAR GENETICS; PHENOTYPE;

AMINO ACID SUBSTITUTION; ANEMIA, HYPOCHROMIC; CATION TRANSPORT PROTEINS; CODON; FEMALE; FERRITINS; HEMOCHROMATOSIS; HUMANS; MOLECULAR SEQUENCE DATA; MUTATION, MISSENSE; PHENOTYPE; TRANSFERRIN;

EID: 64249083699     PISSN: None     EISSN: 14321203     Source Type: Journal    
DOI: None     Document Type: Article

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