A loss-of-function mutation in natriuretic peptide receptor 2 (Npr2) gene is responsible for disproportionate dwarfism in cn/cn mouse (Q28235995)
Jump to navigation
Jump to search
scientific article (publication date: 8 April 2005)
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | A loss-of-function mutation in natriuretic peptide receptor 2 (Npr2) gene is responsible for disproportionate dwarfism in cn/cn mouse |
scientific article (publication date: 8 April 2005) |
Statements
A loss-of-function mutation in natriuretic peptide receptor 2 (Npr2) gene is responsible for disproportionate dwarfism in cn/cn mouse (English)
0 references
8 April 2005
0 references
280
0 references
14
0 references
14288-92
0 references
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference