1998-05-11
Homozygous R788W point mutation in the XPF gene of a patient with xeroderma pigmentosum and late-onset neurologic disease
Publication
Publication
The Journal of Investigative Dermatology , Volume 110 - Issue 5 p. 832- 836
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doi.org/10.1046/j.1523-1747.1998.00171.x, hdl.handle.net/1765/62289 | |
The Journal of Investigative Dermatology | |
Organisation | Department of Clinical Genetics |
Sijbers, A., van Voorst Vader, P., Snoek, J., Raams, A., Jaspers, N., & Kleijer, W. (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 |