Whole-exome sequencing identifies novel autosomal recessive DSG1 mutations associated with mild SAM syndrome
Schlipf, N.A., Vahlquist, A., Teigen, N., Virtanen, M., Dragomir, A., Fismen, S., Barenboim, M., Manke, T., Rösler, B., Zimmer, A., Fischer, J.Volume:
174
Language:
english
Journal:
British Journal of Dermatology
DOI:
10.1111/bjd.14079
Date:
February, 2016
File:
PDF, 684 KB
english, 2016