## Abstract Cowden disease (CD) is an autosomal dominant syndrome characterized by multiple hamartomatous lesions and an increased risk for malignancies. Recent evidence has indicated that the PTEN gene, encoding a protein tyrosine phosphatase, is the CD susceptibility gene. However, another line o
โฆ LIBER โฆ
Novel mutation of L718X in theATP7Agene in a Japanese patient with classical Menkes disease, and four novel polymorphisms in the Japanese population
โ Scribed by A. Ogawa; S. Yamamoto; M. Kanazawa; E. Ogawa; M. Takayanagi; S. Hasegawa; Y. Kohno
- Publisher
- Nature Publishing Group
- Year
- 2000
- Tongue
- English
- Weight
- 77 KB
- Volume
- 45
- Category
- Article
- ISSN
- 1435-232X
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