MeSH Review:
Hair Diseases
- Mutations in the hair cortex keratin hHb6 cause the inherited hair disease monilethrix. Winter, H., Rogers, M.A., Langbein, L., Stevens, H.P., Leigh, I.M., Labrèze, C., Roul, S., Taieb, A., Krieg, T., Schweizer, J. Nat. Genet. (1997)
- Structural changes of hair after incorporation of the proline analogue L-azetidine-2-carboxylic acid. A model of hair disease by alteration of primary structure. Lubec, G., Pollak, A., Coradello, H., Aschinger, H., Wagendristl, A., Bangert, H., Seifert, K., Ratzenhofer, E. Wien. Klin. Wochenschr. (1985)









