Syndromic congenital myelofibrosis associated with a loss-of-function variant in RBSN.
Blood
; 132(6): 658-662, 2018 08 09.
Article
in En
| MEDLINE
| ID: mdl-29784638
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Vesicular Transport Proteins
/
Primary Myelofibrosis
Type of study:
Risk_factors_studies
Limits:
Child
/
Female
/
Humans
/
Infant
/
Male
Language:
En
Journal:
Blood
Year:
2018
Document type:
Article
Country of publication:
Estados Unidos