A physical complex of the Fanconi anemia proteins FANCG/XRCC9 and FANCA

Fanconi anemia (FA) is a recessively inherited disease characterized at the cellular level by spontaneous chromosomal instability and specific hypersensitivity to cross-linking agents. FA is genetically heterogeneous, comprising at least eight complementation groups (A-H). We report that the protein...

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Bibliografiset tiedot
Päätekijät: Waisfisz, Quinten, de Winter, Johan P., Kruyt, Frank A. E., de Groot, Jan, van der Weel, Laura, Dijkmans, Lonneke M., Zhi, Yu, Arwert, Fré, Scheper, Rik J., Youssoufian, Hagop, Hoatlin, Maureen E., Joenje, Hans
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: The National Academy of Sciences 1999
Aiheet:
Biological Sciences
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC17886/
https://ncbi.nlm.nih.gov/pubmed/10468606
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