Whole exome sequencing identified five novel variants in CNTN2, CARS2, ARSA, and CLCN4 leading to epilepsy in consanguineous families.
Front Genet
; 14: 1185065, 2023.
Article
in En
| MEDLINE
| ID: mdl-37359369
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01-internacional
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MEDLINE
Type of study:
Guideline
Language:
En
Journal:
Front Genet
Year:
2023
Document type:
Article
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