Homozygous R788W point mutation in the XPF gene of a patient with xeroderma pigmentosum and late-onset neurologic disease

AM (Anneke) Sijbers, PC van Voorst Vader, JW Snoek, Anja Raams, Koos Jaspers, W Kleijer

Research output: Contribution to journalArticleAcademicpeer-review

54 Citations (Scopus)
Original languageUndefined/Unknown
Pages (from-to)832-836
Number of pages5
JournalJournal of Investigative Dermatology
Publication statusPublished - 1998

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