Polymorphisms and mutations of human TMPRSS6 in iron deficiency anemia

Blood Cells, Molecules, and Diseases

Volumn 44, Issue 1, 2010, Pages 16-21

  Beutler, E ^a   Van Geet, C ^b   te Loo, D M W M ^c   Gelbart, T ^a   Crain, K ^a   Truksa, J ^a   Lee, P L ^a  

^a SCRIPPS RESEARCH INSTITUTE   (United States)

^b UNIVERSITY HOSPITALS LEUVEN   (Belgium)

^c RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

Anemia; Hepcidin; Iron deficiency; Matriptase; TMPRSS6

Indexed keywords

HEPCIDIN; IRON; IRON SORBITEX; PROTEIN TMPRSS6; SERINE PROTEINASE; UNCLASSIFIED DRUG;

ADOLESCENT; ADULT; ARTICLE; CHILD; CONTROLLED STUDY; FEMALE; FRAMESHIFT MUTATION; GENE DELETION; GENETIC ASSOCIATION; GENETIC POLYMORPHISM; GENETIC RISK; HETEROZYGOTE; HUMAN; IRON DEFICIENCY ANEMIA; LABORATORY TEST; MAJOR CLINICAL STUDY; MALE; MOTHER; MUTATION RATE; MUTATIONAL ANALYSIS; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SCHOOL CHILD; SIBLING; SPLICING DEFECT; URINE LEVEL;

AGED; AMINO ACID SUBSTITUTION; ANEMIA, IRON-DEFICIENCY; ANEMIA, REFRACTORY; ANTIMICROBIAL CATIONIC PEPTIDES; CHILD; COHORT STUDIES; DNA MUTATIONAL ANALYSIS; EUROPEAN CONTINENTAL ANCESTRY GROUP; FEMALE; GENE FREQUENCY; HEP G2 CELLS; HUMANS; INFANT; MALE; MEMBRANE PROTEINS; MIDDLE AGED; MUTATION; PEDIGREE; POLYMORPHISM, GENETIC; SERINE ENDOPEPTIDASES;

EID: 72649088708     PISSN: 10799796     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bcmd.2009.09.001     Document Type: Article

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