And at most a single deleterious mutation in the unaffected sibling. No
And at most one deleterious mutation in the unaffected sibling. No such genes or variants have been located. We did identify a novel heterozygous G to A transition within exon…
And at most one deleterious mutation in the unaffected sibling. No such genes or variants have been located. We did identify a novel heterozygous G to A transition within exon…
Oss of MLH1 in this context is most likely a result of promoter hypermethylation. We observed no relationship amongst sidedness and MLH1 methylation or protein expression loss, nor was genotype…