## 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
✦ LIBER ✦
Novel PTEN mutations in patients with Cowden disease: absence of clear genotype–phenotype correlations
✍ Scribed by Nelen, Marcel R; Kremer, Hannie; Konings, Irene BM; Schoute, Frans; Essen, Anton J van; Koch, Rainer; Woods, C Geoffrey; Fryns, Jean-Pierre; Hamel, Ben; Hoefsloot, Lies H
- Book ID
- 110024797
- Publisher
- Nature Publishing Group
- Year
- 1999
- Tongue
- English
- Weight
- 216 KB
- Volume
- 7
- Category
- Article
- ISSN
- 1018-4813
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