Our finding that ADHD + CP can represent a familial distinct subtype possibly with
a distinct genetic etiology is consistent with a high risk for cosegregation.
176/6: 15 The genetics of emphysema: Mutations in telomere genes uncover
a distinct genetic etiology and common mechanism for pathogenesis.
Not exact matches
It is classified as a
distinct primary cardiomyopathy with a
genetic etiology and may be an isolated finding or may also be associated with other forms of structural congenital heart disease (Jenni et al., 2001).