A R Lehmann

Characterization of a novel human SMC heterodimer homologous to the Schizosaccharomyces pombe Rad18/Spr18 complex.

P B Moens, A. Lehmann, P. Moens, 2001, Molecular biology of the cell.

Analysis of mutations in the XPD gene in Italian patients with trichothiodystrophy: site of mutation correlates with repair deficiency, but gene dosage appears to determine clinical severity.

A. Lehmann, M. Stefanini, T. Nardò, 1998, American journal of human genetics.

The xeroderma pigmentosum group D (XPD) gene: one gene, two functions, three diseases.

A. Lehmann, A R Lehmann, 2001, Genes & development.