A nonsense variant in KRT31 is associated with autosomal dominant monilethrix. Xiong X, Cesarato N, Gossmann Y, Wehner M, et al. Br J Dermatol 2024;191:979-987.

Read + Share

Amedeo Smart

Independent Medical Education

Read + Share

Xiong X, Cesarato N, Gossmann Y, Wehner M, et al. A nonsense variant in KRT31 is associated with autosomal dominant monilethrix. Br J Dermatol 2024;191:979-987.
PMID: 39026424