Loss of expression of FANCD2 protein in sporadic and hereditary breast cancer
Fanconi anemia (FA) is a recessive disorder associated with progressive pancytopenia, multiple developmental defects, and marked predisposition to malignancies. FA is genetically heterogeneous, comprising at least 12 complementation groups (A–M). Activation of one of the FA proteins (FANCD2) by mono...
| Main Authors: | , , , , , |
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| Format: | Online |
| Language: | English |
| Published: |
Springer US
2007
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| Online Access: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2096638/ |