Parental mosaicism and autosomal dominant mutations causing structural abnormalities of collagen I are frequent in families with osteogenesis imperfecta type III/IV.
Acta Paediatr. 1997 Jul;86(7):711-8. doi: 10.1111/j.1651-2227.1997.tb08573.x.
Acta Paediatr. 1997.
PMID: 9240878