Abstract
Darier’s disease (DD, MIM 124200) is an autosomal dominant inherited disease. It is usually present in teenagers or adults with multiple keratotic papules or plaques in seborrheic areas. Pathogenic mutations in the ATP2A2 gene have been identified. It encodes the sarcoplasmic or endoplasmic reticulum Ca2+ ATPase isoform 2 (SERCA2). Polymerase chain reaction and direct sequencing of the full coding sequence of ATP2A2 gene were performed to identify the mutation in this family. In this report, we identified a novel mutation of ATP2A2 gene in a Chinese family with DD. It is a novel heterozygous nucleotide G → T transition at position 2,282 in exon 15 of the ATP2A2 gene. Our study expands the database on the ATP2A2 gene mutations in DD.
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Acknowledgments
We are most grateful to all members of family for participating in this study. We would like to express our thanks to Tao Yang and Yingmin Liu for their help.
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Song, J., Li, M., Yang, LJ. et al. Identification a novel missense mutation p.R761L in Chinese patients with Darier’s disease. Arch Dermatol Res 302, 311–314 (2010). https://doi.org/10.1007/s00403-010-1042-7
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DOI: https://doi.org/10.1007/s00403-010-1042-7