151 Complex phenotypes in trichothiodystrophy patients with XPD (ERCC2) mutations

Autor: Jeskey, J., Rizza, E.H., Sarihan, M., Khan, S.G., Boyle, J., Tamura, D., Mendelsohn, N., Brooks, B.P., Merideth, M., DiGiovanna, J.J., Kraemer, K.H.
Zdroj: In Journal of Investigative Dermatology May 2021 141(5) Supplement:S27-S27
Databáze: ScienceDirect