Learning from a paradox: recent insights into Fanconi anaemia through studying mouse models
Fanconi anaemia (FA) is a rare autosomal recessive or X-linked inherited disease characterised by an increased incidence of bone marrow failure (BMF), haematological malignancies and solid tumours. Cells from individuals with FA show a pronounced sensitivity to DNA interstrand crosslink (ICL)-induci...
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| Main Authors: | , , |
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| Format: | Book |
| Published: |
The Company of Biologists,
2013-01-01T00:00:00Z.
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Internet
Connect to this object online.3rd Floor Main Library
| Call Number: |
A1234.567 |
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| Copy 1 | Available |