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4. C01 Glutamine codon usage and somatic mosaicism of the HTT cag repeat are modifiers of huntington disease severity. (September 2018)

6. C06 Genetic variation in MSH3 that lowers its expression ameliorates disease course and limits repeat expansion in huntington's disease and myotonic dystrophy type 1. (September 2018)

10. Repeat Detector: versatile sizing of expanded tandem repeats and identification of interrupted alleles from targeted DNA sequencing. Issue 4 (5th December 2022)