Familial hypercatabolic hypoproteinemia caused by deficiency of the neonatal Fc receptor, FcRn, due to a mutant beta2-microglobulin gene (Q34596901)
Jump to navigation
Jump to search
scholarly article
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Familial hypercatabolic hypoproteinemia caused by deficiency of the neonatal Fc receptor, FcRn, due to a mutant beta2-microglobulin gene |
scholarly article |
Statements
1 reference
Familial hypercatabolic hypoproteinemia caused by deficiency of the neonatal Fc receptor, FcRn, due to a mutant beta2-microglobulin gene (English)
1 reference
Manzoor A Wani
1 reference
Lynn D Haynes
1 reference
Jonghan Kim
1 reference
C L Bronson
1 reference
Chaity Chaudhury
1 reference
Sudhasri Mohanty
1 reference
Thomas A Waldmann
1 reference
John M Robinson
1 reference
Clark L Anderson
1 reference
20 March 2006
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
Identifiers
1 reference