Homozygous R788W point mutation in the XPF gene of a patient with xeroderma pigmentosum and late-onset neurologic disease (Q42454862)

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scientific article published on May 1998
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Homozygous R788W point mutation in the XPF gene of a patient with xeroderma pigmentosum and late-onset neurologic disease
scientific article published on May 1998

    Statements

    Homozygous R788W point mutation in the XPF gene of a patient with xeroderma pigmentosum and late-onset neurologic disease (English)
    Sijbers AM
    van Voorst Vader PC
    Snoek JW
    Jaspers NG
    Kleijer WJ
    832-836

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