In:
Clinical Chemistry and Laboratory Medicine (CCLM), Walter de Gruyter GmbH, Vol. 42, No. 1 ( 2004-01-16)
Abstract:
Hereditary haemochromatosis is an autosomal recessive disorder of iron regulation that results in abnormal intestinal iron absorption with progressive iron overloading of parenchymal cells. Two specific, single point mutations of the
Type of Medium:
Online Resource
ISSN:
1437-4331
,
1434-6621
DOI:
10.1515/CCLM.2004.005
Language:
Unknown
Publisher:
Walter de Gruyter GmbH
Publication Date:
2004
detail.hit.zdb_id:
1492732-9
SSG:
15,3