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Identification of novel target genes involved in Indian Fanconi anemia patients using microarray

✍ Scribed by Shyamsunder, Pavithra; Ganesh, Kripa S.; Vidyasekar, Prasanna; Mohan, Sheila; Verma, Rama Shanker

Book ID: 122436430
Publisher: Elsevier Science
Year: 2013
Tongue: English
Weight: 715 KB
Volume: 531
Category: Article
ISSN: 0378-1119
DOI: 10.1016/j.gene.2013.08.082

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Fanconi anemia (FA) is a rare autosomal recessive disorder of hematopoiesis, with at least 11 complementation groups. FANCA, a gene for group A, accounts for the majority of FA patients. Previous studies of FANCA mutations revealed high allelic heterogeneity, frequent occurrence of large deletions,

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