(Q42454862)
Statements
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Homozygous R788W point mutation in the XPF gene of a patient with xeroderma pigmentosum and late-onset neurologic disease (English)
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Sijbers AM
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van Voorst Vader PC
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Snoek JW
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Raams A
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Jaspers NG
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Kleijer WJ
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1 May 1998
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110
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5
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832-836
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Identifiers
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1 reference