A novel Leu153Ser mutation of the Fanconi anemia FANCD2 gene is associated with severe chemotherapy...
A novel Leu153Ser mutation of the Fanconi anemia FANCD2 gene is associated with severe chemotherapy toxicity in a pediatric T-cell acute lymphoblastic leukemia
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Author / Creator
Borriello, A , Locasciulli, A , Bianco, A M , Criscuolo, M , Conti, V , Grammatico, P , Cappellacci, S , Zatterale, A , Morgese, F , Cucciolla, V , Delia, D , Ragione, F Della and Savoia, A
Publisher
London: Nature Publishing
Journal title
Language
English
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Publication information
Publisher
London: Nature Publishing
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Scope and Contents
Contents
Fanconi anemia (FA) is an autosomal recessive disease characterized by pancitopenia, congenital malformations, predisposition to cancers and chromosomal instability. We report the clinical and molecular features of a patient initially identified as a potential FA case only because of chemotherapy toxicity during the treatment of a T-lineage acute l...
Alternative Titles
Full title
A novel Leu153Ser mutation of the Fanconi anemia FANCD2 gene is associated with severe chemotherapy toxicity in a pediatric T-cell acute lymphoblastic leukemia
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Record Identifier
TN_cdi_proquest_miscellaneous_817604094
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_817604094
Other Identifiers
ISSN
0887-6924
E-ISSN
1476-5551
DOI
10.1038/sj.leu.2404468
