Severe hemolytic anemia in a newborn: Look out for rare Gardos channelopathies due to KCNN4 mutation.
Vania MunarettoMaddalena MartellaSamuela FrancescatoGiulia ReggianiMaria Paola BoaroPaola BianchiElisa FermoWilma BarcelliniLaura SainatiRaffaella ColombattiPublished in: Pediatric blood & cancer (2023)