A novel homozygous SCO2 mutation, p.G193S, causing fatal infantile cardioencephalomyopathy (Q44992179)
Jump to navigation
Jump to search
scientific article
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | A novel homozygous SCO2 mutation, p.G193S, causing fatal infantile cardioencephalomyopathy |
scientific article |
Statements
1 reference
A novel homozygous SCO2 mutation, p.G193S, causing fatal infantile cardioencephalomyopathy (English)
1 reference
Mobley BC
1 reference
Enns GM
1 reference
Wong LJ
1 reference
Vogel H
1 reference
1 March 2009
1 reference
1 reference
28
1 reference
2
1 reference
143-149
1 reference
Identifiers
1 reference