J. Nico P. de Villiers

Spectrum of Mutations in the HFE Gene Implicated in Haemochromatosis and Porphyria

J. Nico P. de Villiers, Renate Hillermann, L. Loubser et al. · Human Molecular Genetics · 1999 · 84 citations · Full text

Analysis of the NRAMP1 Gene Implicated in Iron Transport: Association with Multiple Sclerosis and Age Effects

Maritha J. Kotze, J. Nico P. de Villiers, Roberta N. Rooney et al. · Blood Cells Molecules and Diseases · 2001 · 73 citations

Neurodegenerative Diseases, Disease Mechanism, Neurological Disorder +7

A Reverse-Hybridization Assay for the Rapid and Simultaneous Detection of Nine <i>HFE</i> Gene Mutations

Christian Oberkanins, Anne Moritz, J. Nico P. de Villiers et al. · Genetic Testing · 2000 · 55 citations

Founder mutations in the LDL receptor gene contribute significantly to the familial hypercholesterolemia phenotype in the indigenous South African population of mixed ancestry

Odell Loubser, A. David Marais, Maritha J. Kotze et al. · Clinical Genetics · 1999 · 33 citations

CpG hotspot mutations at the LDL receptor locus are a frequent cause of familial hypercholesterolemia among South African Indians

Maritha J. Kotze, Odell Loubser, Rochelle Thiart et al. · Clinical Genetics · 1997 · 28 citations

South African Indians, Genetics, Genetic Epidemiology +19