, ,
doi.org/10.1046/j.1523-1747.1998.00171.x, hdl.handle.net/1765/62289
The Journal of Investigative Dermatology
Department of Clinical Genetics

Sijbers, A.M, van Voorst Vader, P.C, Snoek, J.W, Raams, A, Jaspers, N.G.J, & Kleijer, W.J. (1998). Homozygous R788W point mutation in the XPF gene of a patient with xeroderma pigmentosum and late-onset neurologic disease. The Journal of Investigative Dermatology, 110(5), 832–836. doi:10.1046/j.1523-1747.1998.00171.x