Characterisation of de novo MAPK10/JNK3 truncation mutations associated with cognitive disorders in two unrelated patients.
Hum Genet
; 132(4): 461-71, 2013 Apr.
Article
in En
| MEDLINE
| ID: mdl-23329067
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Seizures
/
Translocation, Genetic
/
Amino Acid Sequence
/
Sequence Deletion
/
Mitogen-Activated Protein Kinase 10
/
Intellectual Disability
Type of study:
Prognostic_studies
/
Risk_factors_studies
Language:
En
Journal:
Hum Genet
Year:
2013
Document type:
Article
Affiliation country:
Germany
Country of publication:
Germany