Relevance of biallelic versus monoallelic TNFRSF13B mutations in distinguishing disease-causing from risk-increasing TNFRSF13B variants in antibody deficiency syndromes (Q37116935)
Jump to navigation
Jump to search
scientific article
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Relevance of biallelic versus monoallelic TNFRSF13B mutations in distinguishing disease-causing from risk-increasing TNFRSF13B variants in antibody deficiency syndromes |
scientific article |
Statements
1 reference
Relevance of biallelic versus monoallelic TNFRSF13B mutations in distinguishing disease-causing from risk-increasing TNFRSF13B variants in antibody deficiency syndromes (English)
1 reference
Hans D Ochs
1 reference
Lennart Hammarström
1 reference
Bodo Grimbacher
1 reference
Alejandro A Schäffer
1 reference
Alessandro Plebani
1 reference
Vassilis Lougaris
1 reference
Jennifer Birmelin
1 reference
Astrid Bergbreiter
1 reference
Simon Urschel
1 reference
Chiara Bacchelli
1 reference
Tina Hagena
1 reference
Sylvie Buckridge
1 reference
Qiang Pan-Hammarström
1 reference
Stephanie Jennings
1 reference
A David B Webster
1 reference
Hans-Hartmut Peter
1 reference
Daniel Suez
1 reference
Helen Chapel
1 reference
Andrew McLean-Tooke
1 reference
Gavin P Spickett
1 reference
Stephanie Anover-Sombke
1 reference
Bernd H Belohradsky
1 reference
Sanja Ugrinovic
1 reference
Dinakantha S Kumararatne
1 reference
Tatiana C Lawrence
1 reference
Are M Holm
1 reference
Jose L Franco
1 reference
Ilka Schulze
1 reference
E Michael Gertz
1 reference
H Bobby Gaspar
1 reference
3 November 2008
1 reference
1 reference
1967-1976
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
Identifiers
1 reference
1 reference
1 reference