Single-cell genome sequencing of human neurons identifies somatic point mutation and indel enrichment in regulatory elements.
Nat Genet
; 54(10): 1564-1571, 2022 10.
Article
in En
| MEDLINE
| ID: mdl-36163278
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Point Mutation
/
High-Throughput Nucleotide Sequencing
Limits:
Humans
Language:
En
Journal:
Nat Genet
Journal subject:
GENETICA MEDICA
Year:
2022
Document type:
Article
Affiliation country:
Estados Unidos
Country of publication:
Estados Unidos