https://eprints.ncl.ac.uk/81103
Distinct mutations in human basic hair keratins 1 and 6 cause monilethrix: Implications for protein...
https://pubmed.ncbi.nlm.nih.gov/12653715/
Recurrent missense mutations in the hair keratin gene hHb6 in monilethrix
Monilethrix is an autosomal dominant hair disorder characterized by a beaded appearance of the hair resulting from periodic thinning of the shaft (MIM 158000)....
in thehair keratinrecurrentmutationsgene