Fanconi anemia with sun-sensitivity caused by a Xeroderma pigmentosum-associated missense mutation in XPF.
Authors
Popp, IPunekar, M
Telford, Nicholas
Stivaros, S
Chandler, K
Minnis, M
Castleton, Anna
Higham, Claire E
Hopewell, L
Evans, D
Raams, A
Theil, A
Meyer, Stefan
Schindler, D
Affiliation
Department of Human Genetics, Biozentrum, University of Wurzburg, Am Hubland, 97074, Wurzburg, GermanyIssue Date
2018-01-11
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Show full item recordAbstract
Fanconi anemia (FA) is an inherited genomic instability disorder with congenital and developmental abnormalities, bone marrow failure and predisposition to cancer early in life, and cellular sensitivity to DNA interstrand crosslinks.Citation
Fanconi anemia with sun-sensitivity caused by a Xeroderma pigmentosum-associated missense mutation in XPF. 2018, 19 (1):7 BMC Med GenetJournal
BMC Medical GeneticsDOI
10.1186/s12881-018-0520-1PubMed ID
29325523Type
ArticleLanguage
enISSN
1471-2350ae974a485f413a2113503eed53cd6c53
10.1186/s12881-018-0520-1
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