We report the genetic analysis of a large multi-generational family composed of 144 individuals in which 11 members have been diagnosed with chronic lymphocytic leukaemia (CLL). The observation of a significant over-representation of monoclonal B-cell lymphocytosis (MBL) in unaffected family members strongly supports MBL being a surrogate marker of carrier status. A genome-wide linkage scan of the family using high-density 10K single nucleotide polymorphisms provided no significant evidence for a single gene model of disease susceptibility, inviting speculation that susceptibility to CLL has a more complex basis. The absence of a correlation in IGHV usage between affected family members does however argue strongly against exposure to a single super-antigen in disease development. © 2008 The Authors.
CITATION STYLE
Fuller, S. J., Papaemmanuil, E., McKinnon, L., Webb, E., Sellick, G. S., Dao-Ung, L. P., … Wiley, J. S. (2008). Analysis of a large multi-generational family provides insight into the genetics of chronic lymphocytic leukemia. British Journal of Haematology, 142(2), 238–245. https://doi.org/10.1111/j.1365-2141.2008.07188.x
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