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Updated: Jun 17, 2026

09:34
Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional Disease
Published on: April 4, 2018
Three-base deletion mutation c.120_122delGTT in ATP2A2 leads to the unique phenotype of comedonal Darier disease
D Tsuruta1, M Akiyama, A Ishida-Yamamoto
1Department of Dermatology, Osaka City University Graduate School of Medicine, Osaka, Japan.
The British Journal of Dermatology
|December 10, 2009
Abstract
No abstract available in PubMed .
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