L. Quintana

Transferrin receptor mutation analysis in hereditary hemochromatosis patients.

R. Wolff, F. Mapa, Z. Tsuchihashi, 1998, Blood cells, molecules & diseases.

A novel MHC class I–like gene is mutated in patients with hereditary haemochromatosis

M. C. Ellis, A. Gnirke, N. Risch, 1996, Nature Genetics.

Cloning of a Unique Lipase from Endothelial Cells Extends the Lipase Gene Family*

Sungshin Y. Choi, T. Quertermous, N. Leeper, 1999, The Journal of Biological Chemistry.

HLA class II haplotype and sequence analysis support a role for DQ in narcolepsy

M. C. Ellis, M. Aldrich, E. Mignot, 1997, Immunogenetics.

A 1.1-Mb transcript map of the hereditary hemochromatosis locus.

R. Wolff, F. Mapa, D. Ruddy, 1997, Genome research.