Detalhe da pesquisa
1.
Insight into the phenotype of infants with Pompe disease identified by newborn screening with the common c.-32-13T>G "late-onset" GAA variant.
Mol Genet Metab
; 122(3): 99-107, 2017 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-28951071