A mutation in SLC11A3 is associated with autosomal dominant hemochromatosis

Nature Genetics

Volumn 28, Issue 3, 2001, Pages 213-214

  Njajou, Omer T ^a   Vaessen, Norbert ^a   Joosse, Marijke ^a   Berghuis, Bianca ^a   Van Dongen, Jeroen W F ^a   Breuning, Martijn H ^b   Snijders, Pieter J L M ^a   Rutten, Wim P F ^c   Sandkuijl, Lodewijk A ^a   Oostra, Ben A ^a   Van Duijn, Cornelia M ^a   Heutink, Peter ^a  

^a ERASMUS UNIVERSITY ROTTERDAM   (Netherlands)

^b LEIDEN UNIVERSITY MEDICAL CENTER   (Netherlands)

^c Stichting Huisarts Laboratorium Breda   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CLINICAL ARTICLE; CONTROLLED STUDY; FEMALE; GENE MUTATION; HEMOCHROMATOSIS; HUMAN; HUMAN TISSUE; IRON OVERLOAD; LIVER BIOPSY; MALE; PRIORITY JOURNAL;

AMINO ACID SEQUENCE; CARRIER PROTEINS; CATION TRANSPORT PROTEINS; FEMALE; FERRITINS; GENES, DOMINANT; HEMOCHROMATOSIS; HUMANS; LINKAGE (GENETICS); MALE; MOLECULAR SEQUENCE DATA; MUTATION; PEDIGREE; SEQUENCE HOMOLOGY, AMINO ACID; TRANSFERRIN;

EID: 0034930197     PISSN: 10614036     EISSN: None     Source Type: Journal    
DOI: 10.1038/90038     Document Type: Article

References (15)