Mark L - Rare Diseases Clinical Research Network
This is particularly cumbersome for investigating rare diseases, such as large granular lymphocyte (LGL) leukemia, where sample size is extremely small. Methods: A cohort of LGL patients (n=37) were analyzed for SNPs that co-segregate with disease versus controls (n=56) using the Illumina 12K non-synonymous SNP genotyping platform. ................
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