Identification by next-generation sequencing of 2 novel cases of noncompaction cardiomyopathy associated with 1p36 deletions.
Rev Esp Cardiol (Engl Ed)
; 73(9): 780-782, 2020 Sep.
Article
in En, Es
| MEDLINE
| ID: mdl-32192878
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
High-Throughput Nucleotide Sequencing
/
Cardiomyopathies
Type of study:
Diagnostic_studies
/
Prognostic_studies
/
Risk_factors_studies
Limits:
Humans
Language:
En
/
Es
Journal:
Rev Esp Cardiol (Engl Ed)
Year:
2020
Document type:
Article