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 journal › Article › Academic › peer-review

54 Citations (Scopus)

Original language	Undefined/Unknown
Pages (from-to)	832-836
Number of pages	5
Journal	Journal of Investigative Dermatology
Volume	110
DOIs	https://doi.org/10.1046/j.1523-1747.1998.00171.x
Publication status	Published - 1998

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

author = "Sijbers, {AM (Anneke)} and {van Voorst Vader}, PC and JW Snoek and Anja Raams and Koos Jaspers and W Kleijer",

year = "1998",

doi = "10.1046/j.1523-1747.1998.00171.x",

language = "Undefined/Unknown",

volume = "110",

pages = "832--836",

journal = "Journal of Investigative Dermatology",

issn = "0022-202X",

publisher = "Nature Publishing Group",

}

TY - JOUR

T1 - Homozygous R788W point mutation in the XPF gene of a patient with xeroderma pigmentosum and late-onset neurologic disease

AU - Sijbers, AM (Anneke)

AU - van Voorst Vader, PC

AU - Snoek, JW

AU - Raams, Anja

AU - Jaspers, Koos

AU - Kleijer, W

PY - 1998

Y1 - 1998

U2 - 10.1046/j.1523-1747.1998.00171.x

DO - 10.1046/j.1523-1747.1998.00171.x

M3 - Article

SN - 0022-202X

VL - 110

SP - 832

EP - 836

JO - Journal of Investigative Dermatology

JF - Journal of Investigative Dermatology

ER -