Whole-body MRI evaluation in neurofibromatosis type 1 patients younger than 3 years old and the genetic contribution to disease progression.
Orphanet J Rare Dis
; 17(1): 24, 2022 01 29.
Article
in En
| MEDLINE
| ID: mdl-35093157
Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Neurofibromatosis 1
Type of study:
Observational_studies
Limits:
Child
/
Humans
Language:
En
Journal:
Orphanet J Rare Dis
Journal subject:
MEDICINA
Year:
2022
Document type:
Article