𝔖 Bobbio Scriptorium
✦   LIBER   ✦

0226 Report of Cowden's syndrome in patient with PTEN mutation

✍ Scribed by I. Melbarde-Gorkusa; A. Irmejs; E. Miklasevics; I. Strumfa; B. Vagule; I. Grinfelde; J. Gardovskis; S. Subatniece; A. Gardovskis


Book ID
114316349
Publisher
Elsevier Science
Year
2009
Tongue
English
Weight
50 KB
Volume
18
Category
Article
ISSN
0960-9776

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


PTEN mutation in a family with Cowden sy
✍ Goffin, Aleide ;Hoefsloot, Lies H. ;Bosgoed, Ermanno ;Swillen, Ann ;Fryns, Jean- πŸ“‚ Article πŸ“… 2001 πŸ› John Wiley and Sons 🌐 English βš– 107 KB πŸ‘ 2 views
A novel PTEN mutation in a Japanese pati
✍ Y. Kubo; Y. Urano; Y. Hida; T. Ikeuchi; M. Nomoto; K. Kunitomo; S. Arase πŸ“‚ Article πŸ“… 2000 πŸ› John Wiley and Sons 🌐 English βš– 446 KB

## 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