Hereditary hemochromatosis: A HpaI polymorphism within the HLA-H gene

Molecular and Cellular Probes

Volumn 11, Issue 3, 1997, Pages 229-230

  Totaro, A ^a   Grifa, A ^a   Carella, M ^a   D'Ambrosio, L ^a   Valentino, M ^a   Roth, M P ^b   Borot, N ^b   Coppin, H ^b   Roetto, A ^c   Camaschella, C ^c   Gasparini, P ^a  

^a CASA SOLLIEVO DELLA SOFFERENZA HOSPITAL   (Italy)

^b Ctr de Immunopathologie et de G   (France)

^c SAN LUIGI GONZAGA HOSPITAL   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

HLA ANTIGEN CLASS 1; PRIMER DNA;

ARTICLE; CHROMOSOME 6P; GENE FREQUENCY; GENE MAPPING; HEMOCHROMATOSIS; HISTOCOMPATIBILITY GENE; HUMAN; MAJOR CLINICAL STUDY; NORMAL HUMAN; NUCLEIC ACID BASE SUBSTITUTION; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; RESTRICTION FRAGMENT LENGTH POLYMORPHISM;

EID: 0031170905     PISSN: 08908508     EISSN: None     Source Type: Journal    
DOI: 10.1006/mcpr.1997.0102     Document Type: Article

References (5)

1. 1. Feder, J. N., Gnirke, A., Thomas, W. et a/. (1996). A novel MHC class I like gene is mutated in patients with Hereditary Hemochromatosis. Nature Genetics 13, 399-408.
2. 2. Jazwinska, E., Cullen, L., Busfield, F. et al. (1996). Hemochromatosis and HLA-H. Nature Genetics 14, 249-51.
3. 3. Janouelle, A., Gandon, G., Jezequel, P. et al. (1996). Hemochromatosis and HLA-H. Nature Genetics 14, 251-2.
4. 4. Rothenberg, B. & Voland, J. (1996). β2 knockout mice develop parenchymal iron overload: a putative role for class I genes of the major histocompatibility complex in iron metabolism. Proceedings of the National Academy of Sciences, USA 93, 1529-34.
5. 5. Gasparini, P., Bonizzato, A., Dognini, M. & Pignatti, P. F. (1992). Restriction site generating-polymerase chain reaction (RG-PCR) for the probeless detection of hidden genetic variation: application to the study of some common cystic fibrosis mutations. Molecular and Cellular Probes 6, 1-7.