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    Fanconi anemia with sun-sensitivity caused by a Xeroderma pigmentosum-associated missense mutation in XPF.

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    Authors
    Popp, I
    Punekar, 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
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    Affiliation
    Department of Human Genetics, Biozentrum, University of Wurzburg, Am Hubland, 97074, Wurzburg, Germany
    Issue Date
    2018-01-11
    
    Metadata
    Show full item record
    Abstract
    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 Genet
    Journal
    BMC Medical Genetics
    URI
    http://hdl.handle.net/10541/620823
    DOI
    10.1186/s12881-018-0520-1
    PubMed ID
    29325523
    Type
    Article
    Language
    en
    ISSN
    1471-2350
    ae974a485f413a2113503eed53cd6c53
    10.1186/s12881-018-0520-1
    Scopus Count
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