✦ LIBER ✦
Three-base deletion mutation c.120_122delGTT in ATP2A2 leads to the unique phenotype of comedonal Darier disease
✍ Scribed by D. Tsuruta; M. Akiyama; A. Ishida-Yamamoto; H. Imanishi; N. Mizuno; J. Sowa; H. Kobayashi; M. Ishii; I. Kurokawa; H. Shimizu
- Book ID
- 108671013
- Publisher
- John Wiley and Sons
- Year
- 2010
- Tongue
- English
- Weight
- 298 KB
- Volume
- 162
- Category
- Article
- ISSN
- 0007-0963
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