A Novel FLCN Intragenic Deletion Identified by NGS in a BHDS Family and Literature Review.
Front Genet
; 12: 636900, 2021.
Article
in En
| MEDLINE
| ID: mdl-33927747
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Type of study:
Prognostic_studies
Language:
En
Journal:
Front Genet
Year:
2021
Document type:
Article
Affiliation country:
China
Country of publication:
Switzerland