Tags

Type your tag names separated by a space and hit enter

The HFE Cys282Tyr mutation as a necessary but not sufficient cause of clinical hereditary hemochromatosis.
Blood 2003; 101(9):3347-50Blood

Authors+Show Affiliations

Department of Molecular and Experimental Medicine, Scripps Research Institute, La Jolla, CA 92037, USA. beutler@scripps.edu

Pub Type(s)

Journal Article
Research Support, Non-U.S. Gov't
Research Support, U.S. Gov't, P.H.S.
Review

Language

eng

PubMed ID

12707220

Citation

Beutler, Ernest. "The HFE Cys282Tyr Mutation as a Necessary but Not Sufficient Cause of Clinical Hereditary Hemochromatosis." Blood, vol. 101, no. 9, 2003, pp. 3347-50.
Beutler E. The HFE Cys282Tyr mutation as a necessary but not sufficient cause of clinical hereditary hemochromatosis. Blood. 2003;101(9):3347-50.
Beutler, E. (2003). The HFE Cys282Tyr mutation as a necessary but not sufficient cause of clinical hereditary hemochromatosis. Blood, 101(9), pp. 3347-50.
Beutler E. The HFE Cys282Tyr Mutation as a Necessary but Not Sufficient Cause of Clinical Hereditary Hemochromatosis. Blood. 2003 May 1;101(9):3347-50. PubMed PMID: 12707220.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - The HFE Cys282Tyr mutation as a necessary but not sufficient cause of clinical hereditary hemochromatosis. A1 - Beutler,Ernest, PY - 2003/4/23/pubmed PY - 2003/6/21/medline PY - 2003/4/23/entrez SP - 3347 EP - 50 JF - Blood JO - Blood VL - 101 IS - 9 SN - 0006-4971 UR - https://www.unboundmedicine.com/medline/citation/12707220/full_citation L2 - http://www.bloodjournal.org/cgi/pmidlookup?view=long&pmid=12707220 DB - PRIME DP - Unbound Medicine ER -