Prenatal hydrops fetalis associated with infantile free sialic acid storage disease due to a novel homozygous deletion in the SLC17A5 gene

por Hasnain, Afia, Burnett, Sherri, Agatep, Ronald, Spriggs, Elizabeth, Chodirker, Bernard, Mhanni, Aizeddin (Aziz) A.
Publicado 2021