✦ LIBER ✦
Recurrent p.N767S mutation in the ATP2A2 gene in a Japanese family with haemorrhagic Darier disease clinically mimicking epidermolysis bullosa simplex with mottled pigmentation
✍ Scribed by T. Hamada; S. Yasumoto; T. Karashima; N. Ishii; H. Shimada; Y. Kawano; S. Imayama; J.A. McGrath; T. Hashimoto
- Book ID
- 108669587
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- English
- Weight
- 270 KB
- Volume
- 157
- Category
- Article
- ISSN
- 0007-0963
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