Novel SCNN1A gene splicing-site mutation causing autosomal recessive pseudohypoaldosteronism type 1 (PHA1) in two Italian patients belonging to the same small town
Gregorio Serra(University of Palermo), Giovanni Corsello(Azienda di Rilievo Nazionale ed Alta Specializzazione), Maria Michela D’Alessandro(University of Palermo), Vincenzo Verde(University of Palermo), Maria Cristina Maggio(University of Palermo), Vincenzo Antona(University of Palermo)
The Italian Journal of Pediatrics/Italian journal of pediatrics
June 16, 2021
Cited by 44
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