+ Site Statistics
+ Search Articles
+ PDF Full Text Service
How our service works
Request PDF Full Text
+ Follow Us
Follow on Facebook
Follow on Twitter
Follow on LinkedIn
+ Subscribe to Site Feeds
Most Shared
PDF Full Text
+ Translate
+ Recently Requested

Non HFE-related haemochromatosis: exclusion of the 1q21 zinc-iron regulated transporter-like (ZIRTL) gene in juvenile haemochromatosis



Non HFE-related haemochromatosis: exclusion of the 1q21 zinc-iron regulated transporter-like (ZIRTL) gene in juvenile haemochromatosis



Journal of Hepatology 38(3): 376-377




Please choose payment method:






(PDF emailed within 0-6 h: $19.90)

Accession: 049701419

Download citation: RISBibTeXText

PMID: 12586309

DOI: 10.1016/s0168-8278(02)00426-9


Related references

Exclusion of ZIRTL as candidate gene of juvenile hemochromatosis and refinement of the critical interval on 1q21. Blood Cells Molecules and Diseases 26(3): 205-210, 2000

Normal ZIRTL sequence in juvenile and neonatal haemochromatosis. Journal of Hepatology 36(Suppl. 1): 266, 2002

Iron status markers in hereditary haemochromatosis distinction between individuals being homozygous and heterozygous for the haemochromatosis allele. European Journal of Haematology 47(4): 292-298, 1991

Severe juvenile haemochromatosis (JH) missing HFE gene variants: implications for a second gene locus leading to iron overload. British Journal of Haematology 102(4): 1111-1112, 1998

Severe juvenile haemochromatosis (Jh) miassing Hfe gene variants: implications for a second gene locus leading to iron overload. British Journal of Haematology 102(4): 1111-1112, 1998

Idiopathic haemochromatosis and HLA antigens in Italy: is A3 Bw35 HLA haplotype a marker for idiopathic haemochromatosis gene in north east regions?. Journal of Clinical Pathology 39(2): 125-128, 1986

Reduction of body iron in HFE-related haemochromatosis and moderate iron overload (Mi-Iron): a multicentre, participant-blinded, randomised controlled trial. Lancet. Haematology 4(12): E607-E614, 2017

Hereditary juvenile haemochromatosis: a genetically heterogeneous life- threatening iron-storage disease. Journal of Electron Microscopy 91(9): 607-618, 1998

Hereditary juvenile haemochromatosis: a genetically heterogeneous life-threatening iron-storage disease. Qjm 91(9): 607-618, 1998

Gene symbol: HAMP. Disease: Haemochromatosis, juvenile. Human Genetics 124(3): 313, 2008

A simple genetic test identifies 90% of UK patients with haemochromatosis. The UK Haemochromatosis Consortium. Gut 41(6): 841-844, 1998

A Q312X mutation in the hemojuvelin gene is associated with cardiomyopathy due to juvenile haemochromatosis. European Journal of Heart Failure 10(10): 1001-1006, 2008

A Case of Haemochromatosis.-The Relation of Haemochromatosis to Bronzed Diabetes. Journal of Experimental Medicine 4(3-4): 279-306, 1899

Identification and characterization of the zinc-regulated transporters, iron-regulated transporter-like protein (ZIP) gene family in maize. Bmc Plant Biology 13: 114, 2013

Juvenile haemochromatosis caused by a homozygous Gly320Val mutation in the haemojuvelin gene. Ugeskrift for Laeger 175(16): 1113-1114, 2013