Komorowska A, Rozynkowa D, Lee K W, Renouf D V, Nicholls A C, MacKenzie J, Pope F M
Br Dent J. 1989 Oct 7;167(7):239-43. doi: 10.1038/sj.bdj.4806984.
A case is described of four generations of a Polish family with characteristic features of dentinogenesis imperfecta, who also presented with a variety of generalised connective tissue features, suggestive of a structural gene mutation causing abnormalities in connective tissues other than dentine.
本文描述了一个波兰家族的四代人,他们具有牙本质生成不全的特征,同时还表现出多种全身性结缔组织特征,提示存在一种结构基因突变,导致除牙本质外的结缔组织出现异常。