Deleterious mis-splicing of STK11 caused by a novel single-nucleotide substitution in the 3' polypyrimidine tract of intron five.
Mol Genet Genomic Med
; 8(9): e1381, 2020 09.
Article
in En
| MEDLINE
| ID: mdl-32573125
Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Peutz-Jeghers Syndrome
/
Introns
/
Protein Serine-Threonine Kinases
/
Point Mutation
Type of study:
Prognostic_studies
Limits:
Humans
/
Male
/
Middle aged
Language:
En
Journal:
Mol Genet Genomic Med
Year:
2020
Document type:
Article
Affiliation country:
Denmark
Country of publication:
United States