Constitutional mismatch repair deficiency syndrome with atypical features caused by a homozygous MLH1 missense variant (c.1918C>A, p.(Pro640Thr)): a case report.
Front Oncol
; 13: 1195814, 2023.
Article
in En
| MEDLINE
| ID: mdl-37664053
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Type of study:
Prognostic_studies
Language:
En
Journal:
Front Oncol
Year:
2023
Document type:
Article
Affiliation country:
Túnez
Country of publication:
Suiza