Compound heterozygosity for mutations (W156X and R225W) in SCN5A associated with severe cardiac conduction disturbances and degenerative changes in the conduction system (Q40672037)
Jump to navigation
Jump to search
scientific article published on February 2003
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Compound heterozygosity for mutations (W156X and R225W) in SCN5A associated with severe cardiac conduction disturbances and degenerative changes in the conduction system |
scientific article published on February 2003 |
Statements
1 reference
Compound heterozygosity for mutations (W156X and R225W) in SCN5A associated with severe cardiac conduction disturbances and degenerative changes in the conduction system (English)
1 reference
Arthur A M Wilde
1 reference
Connie R Bezzina
1 reference
Martin B Rook
1 reference
W Antoinette Groenewegen
1 reference
Lucas J Herfst
1 reference
Allard C van der Wal
1 reference
Jan Lam
1 reference
Habo J Jongsma
1 reference
Marcel M A M Mannens
1 reference
1 February 2003
1 reference
1 reference
Identifiers
1 reference