Recurrent c.459 C>A mutation of the PERP gene results in severe Olmsted syndrome with congenital hypotrichosis, atopic dermatitis, and growth retardation

enthalten in: The Journal of Dermatology | 2021

von Song, D. | Ran, X. | Chen, Y. | +4

Novel deletion of the POFUT1 gene associated with multiple seborrheic keratosis Dowling–Degos disease

enthalten in: The Journal of Dermatology | 2021

von Chen, Y. | Li, Z. | Song, D. | +1