Severe hemolytic anemia in a newborn: Look out for rare Gardos channelopathies due to KCNN4 mutation.
Pediatr Blood Cancer
; 70(8): e30325, 2023 Aug.
Article
in En
| MEDLINE
| ID: mdl-37132095
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Channelopathies
/
Anemia, Hemolytic
/
Anemia, Hemolytic, Congenital
Limits:
Humans
/
Newborn
Language:
En
Journal:
Pediatr Blood Cancer
Journal subject:
HEMATOLOGIA
/
NEOPLASIAS
/
PEDIATRIA
Year:
2023
Document type:
Article
Affiliation country:
Italy
Publication country:
EEUU
/
ESTADOS UNIDOS
/
ESTADOS UNIDOS DA AMERICA
/
EUA
/
UNITED STATES
/
UNITED STATES OF AMERICA
/
US
/
USA