# Autosomal dominant monilethrix with incomplete penetrance due to a novel KRT86 mutation in a Chinese family

**Authors:** Ru Dai, Tingting Wang, Xianjie Wu

PMC · DOI: 10.1016/j.abd.2022.12.010 · Anais Brasileiros de Dermatologia · 2024-04-08

## Full-text entities

- **Diseases:** monilethrix (MESH:D056734)

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Source: https://tomesphere.com/paper/PMC11221135