【序号】: 1
【作者】:Camaschella C, Roetto A, Calì A, De Gobbi M, Garozzo G, Carella M, Majorano N,
Totaro A, Gasparini P
【题名】:The gene TFR2 is mutated in a new type of haemochromatosis mapping to 7q22.
【期刊】: Nat Genet.
【年、卷、期、起止页码】:2000 May;25(1):14-5.
【全文链接】:http://www.nature.com/ng/journal/v25/n1/abs/ng0500_14.html
【序号】: 2
【作者】: Aguilar-Martinez P, Esculié-Coste C, Bismuth M, Giansily-Blaizot M, Larrey D,
Schved JF
【题名】: Transferrin receptor-2 gene and non-C282Y homozygous patients with
hemochromatosis.
【期刊】: Blood Cells Mol Dis.
【年、卷、期、起止页码】:2001 Jan-Feb;27(1):290-3.
【全文链接】:http://www.sciencedirect.com/science?_ob=ArticleURL&_udi=B6WBV-45S4K98-
1J&_user=10&_rdoc=1&_fmt=&_orig=search&_sort=d&_docanchor=&view=c&_acct=C000050221&_version
=1&_urlVersion=0&_userid=10&md5=63a3ca071706f6766ea1d2308ec15f1d
【序号】: 3
【作者】: Lee PL, Barton JC
【题名】: Hemochromatosis and severe iron overload associated with compound heterozygosity
for TFR2 R455Q and two novel mutations TFR2 R396X and G792R.
【期刊】: Acta Haematol.
【年、卷、期、起止页码】: 2006;115(1-2):102-5.
【全文链接】:http://content.karger.com/produktedb/produkte.asp?
typ=fulltext&file=AHA20061151_2102
【序号】: 4
【作者】:Le Gac G, Mons F, Jacolot S, Scotet V, Férec C, Frébourg T.
【题名】: Early onset hereditary hemochromatosis resulting from a novel TFR2 gene nonsense
mutation (R105X) in two siblings of north French descent.
【期刊】: Br J Haematol.
【年、卷、期、起止页码】:2004 Jun;125(5):674-8.
【全文链接】:http://www3.interscience.wiley.com/journal/118748030/abstract?
CRETRY=1&SRETRY=0
【序号】: 5
【作者】: Fowler C.
【题名】: Hereditary hemochromatosis: pathophysiology, diagnosis, and management.
【期刊】:Crit Care Nurs Clin North Am.
【年、卷、期、起止页码】: 2008 Jun;20(2):191-201, vi.
【全文链接】:http://www.sciencedirect.com/science?_ob=ArticleURL&_udi=B75J0-4SB7S5R-8&_user=10&_rdoc=1&_fmt=&_orig=search&_sort=d&_docanchor=&view=c&_acct=C000050221&_version=1&_urlVersion=0&_userid=10&md5=27d4e9ddc26d98f3b9d62ae69e104a1b