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Volume 354:1204-1205 March 16, 2006 Number 11
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Familial Cancer Associated with a Polymorphism in ARLTS1

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 by Calin, G. A.
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To the Editor: Calin et al. (April 21, 2005, issue)1 proposed that the truncating sequence change in ARLTS1, G446A (Trp149Stop), predisposes persons to a wide range of malignant conditions including chronic lymphocytic leukemia (CLL). The assertion that this variant predisposes persons to CLL was, however, based on observations from only 17 familial patients of mixed ethnic background.

We conducted an association study to determine if this variant or five other coding single-nucleotide polymorphisms (cSNPs) in ARLTS1 predispose to CLL. We analyzed germ-line DNA from 413 patients with CLL (259 men and 154 women; mean age, 58 years; range, 33 to . . . [Full Text of this Article]


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