Paternal gender specificity and mild phenotypes in Charcot –Marie–Tooth type 1A patients with de novo 17p12 rearrangements

ConclusionThis study suggests that de novo CMT1A patients tend to have milder symptoms and that the paternal ages at child births in the de novo group are higher than those of the non ‐de novo group.
Source: Molecular Genetics & Genomic Medicine - Category: Genetics & Stem Cells Authors: Tags: ORIGINAL ARTICLE Source Type: research