Detalhe da pesquisa
1.
The most common mutation in FKRP causing limb girdle muscular dystrophy type 2I (LGMD2I) may have occurred only once and is present in Hutterites and other populations.
Hum Mutat
; 25(1): 38-44, 2005 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-15580560
2.
Compensation for dystrophin-deficiency: ADAM12 overexpression in skeletal muscle results in increased alpha 7 integrin, utrophin and associated glycoproteins.
Hum Mol Genet
; 12(19): 2467-79, 2003 Oct 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-12915458