A Specific CNOT1 Mutation Results in a Novel Syndrome of Pancreatic Agenesis and Holoprosencephaly through Impaired Pancreatic and Neurological Development.
Am J Hum Genet
; 104(5): 985-989, 2019 05 02.
Article
in En
| MEDLINE
| ID: mdl-31006513
Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Pancreas
/
Pancreatic Diseases
/
Transcription Factors
/
Developmental Disabilities
/
Holoprosencephaly
/
Infant, Newborn, Diseases
/
Mutation
/
Nervous System Diseases
Type of study:
Etiology_studies
Limits:
Animals
/
Female
/
Humans
/
Infant
/
Male
/
Newborn
Language:
En
Journal:
Am J Hum Genet
Year:
2019
Document type:
Article
Affiliation country:
Reino Unido
Country of publication:
Estados Unidos