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Adenomatous transformation in hamartomatous polyps cases of two patients with Peutz–Jeghers Syndrome

✍ Scribed by Ehsen Ben Brahim; Raja Jouini; Olfa Khayat; Naceur Labbène; Meriem Bel Haj Salah; Wafa Koubâa; Mohamed Ben Ayed; Dalila Gargouri; Najib Kaabar; Aschraf Chadli-Debbiche

Publisher
Springer
Year
2009
Tongue
English
Weight
60 KB
Volume
24
Category
Article
ISSN
0179-1958

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Functional analysis of LKB1/STK11 mutant
Functional analysis of LKB1/STK11 mutants and two aberrant isoforms found in Peutz-Jeghers Syndrome patients
✍ J. Boudeau; A. Kieloch; D.R. Alessi; A. Stella; G. Guanti; N. Resta 📂 Article 📅 2003 🏛 John Wiley and Sons 🌐 English ⚖ 382 KB 👁 1 views

Peutz-Jeghers Syndrome (PJS) is thought to be caused by mutations occurring in the widely expressed serine/threonine protein kinase named LKB1/STK11. Recent work has led to the identification of four mutants (R304W, I177N, K175-D176del, L263fsX286) and two novel aberrant LKB1/STK11 cDNA isoforms (r2