Mutation analysis of the Fanconi anemia gene FACC.

Fanconi anemia (FA) is a genetically heterogeneous autosomal recessive disorder characterized by a unique hypersensitivity of cells to DNA cross-linking agents; a gene for complementation group C (FACC) has recently been cloned. We have amplified FACC exons with their flanking intron sequences from...

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Bibliografske podrobnosti
Main Authors: Verlander, P. C., Lin, J. D., Udono, M. U., Zhang, Q., Gibson, R. A., Mathew, C. G., Auerbach, A. D.
Format: Artigo
Jezik:Inglês
Izdano: 1994
Teme:
Research Article
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC1918103/
https://ncbi.nlm.nih.gov/pubmed/8128956
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