Identification of four novel PMM2 mutations in congenital disorders of glycosylation (CDG) Ia French patients (Q24681036)
Jump to navigation
Jump to search
scientific article
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Identification of four novel PMM2 mutations in congenital disorders of glycosylation (CDG) Ia French patients |
scientific article |
Statements
Identification of four novel PMM2 mutations in congenital disorders of glycosylation (CDG) Ia French patients (English)
0 references
August 2000
0 references
37
0 references
8
0 references
579-80
0 references
1 reference