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Clinical characteristics of Peutz-Jeghers syndrome in Korean polyposis patients

✍ Scribed by H. S. Choi; Y. J. Park; E. G. Youk; K.-A. Yoon; J.-L. Ku; N. K. Kim; S. M. Kim; Y. J. Kim; D. J. Moon; J. S. Min; C. J. Park; O. S. Bae; D.-H. Yang; S. H. Jun; E. S. Chung; P. M. Jung; Y. Whang; J.-G. Park

Publisher
Springer
Year
2000
Tongue
English
Weight
25 KB
Volume
15
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 πŸ“‚ Article πŸ“… 2003 πŸ› John Wiley and Sons 🌐 English βš– 382 KB πŸ‘ 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