Detalhe da pesquisa
1.
Egyptian glycogen storage disease type III - identification of six novel AGL mutations, including a large 1.5 kb deletion and a missense mutation p.L620P with subtype IIId.
Clin Chem Lab Med
; 47(10): 1233-8, 2009.
Artigo
em Inglês
| MEDLINE | ID: mdl-19754354