A novel mutation in the STK11 gene causes heritable Peutz-Jeghers syndrome - a case report.
BMC Med Genet
; 18(1): 19, 2017 Feb 23.
Article
in En
| MEDLINE
| ID: mdl-28231849
Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Peutz-Jeghers Syndrome
/
Protein Serine-Threonine Kinases
/
Germ-Line Mutation
Type of study:
Diagnostic_studies
/
Etiology_studies
/
Prognostic_studies
Limits:
Adolescent
/
Humans
/
Male
Language:
En
Journal:
BMC Med Genet
Journal subject:
GENETICA MEDICA
Year:
2017
Type:
Article
Affiliation country:
China