A Novel Splicing Mutation c.335-1 G > A in the Cardiac Transcription Factor NKX2-5 Leads to Familial Atrial Septal Defect Through miR-19 and PYK2.
Stem Cell Rev Rep
; 18(8): 2646-2661, 2022 12.
Article
in En
| MEDLINE
| ID: mdl-35778654
Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
MicroRNAs
/
Induced Pluripotent Stem Cells
/
Heart Septal Defects, Atrial
Type of study:
Prognostic_studies
Limits:
Humans
Language:
En
Journal:
Stem Cell Rev Rep
Year:
2022
Document type:
Article
Country of publication: