Christophe Masmejean

Compound Heterozygotes for Hemochromatosis Gene Mutations: May They Help to Understand the Pathophysiology of the Disease?

Patricia Martínez, C. Biron, F Blanc et al. · Blood Cells Molecules and Diseases · 1997 · 61 citations

Compound Heterozygotes, Mendelian Disorder, Genetic Disorder +7

A novel mutation in the iron responsive element of ferritin L-subunit gene as a cause for hereditary hyperferritinemia-cataract syndrome [letter; comment]

Patricia Aguilar‐Martinez, Christine A. Biron, Christophe Masmejean et al. · Blood · 1996 · 42 citations · Full text

Iron Responsive Element, Novel Mutation, Ophthalmology +7

Simple and Rapid Detection of the Newly Described Mutations in the HLA-H Gene

Patricia Martínez, Ph. Jeanjean, Christophe Masmejean et al. · Blood · 1997 · 33 citations · Full text

Simple and Rapid Detection of the Newly Described Mutations in the HLA-H Gene

Patricia Martínez, Ph. Jeanjean, Christophe Masmejean et al. · Blood · 1997 · 28 citations · Full text

Histocompatibility, Chromatin, Hla +15

Haplotype Analysis of the HFE Gene: Implications for the Origins of Hemochromatosis Related Mutations

Patricia Aguilar‐Martinez, Chloé Thelcide, Philippe Jeanjean et al. · Blood Cells Molecules and Diseases · 1999 · 19 citations

Hfe Gene, Genetic Analysis, Haplotype Determination +7