Chargement en cours...
Germline mutations of the LKB1 (STK11) gene in Peutz-Jeghers patients
Germline mutations of the LKB1 (STK11) serine/threonine kinase gene (chromosome 19p13.3) cause Peutz-Jeghers syndrome, which is characterised by hamartomas of the gastrointestinal tract and typical pigmentation. Peutz-Jeghers syndrome carries an overall risk of cancer that may be up to 20 times that...
Enregistré dans:
| Auteurs principaux: | , , , , , , , , , , , |
|---|---|
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
BMJ Group
1999
|
| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1734361/ https://ncbi.nlm.nih.gov/pubmed/10353780 |
| Tags: |
Ajouter un tag
Pas de tags, Soyez le premier à ajouter un tag!
|