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(Q37116935)

English

Relevance of biallelic versus monoallelic TNFRSF13B mutations in distinguishing disease-causing from risk-increasing TNFRSF13B variants in antibody deficiency syndromes

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Relevance of biallelic versus monoallelic TNFRSF13B mutations in distinguishing disease-causing from risk-increasing TNFRSF13B variants in antibody deficiency syndromes (English)
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Sylvie Buckridge
Qiang Pan-Hammarström
Stephanie Jennings
A David B Webster
Hans-Hartmut Peter
Andrew McLean-Tooke
Gavin P Spickett
Stephanie Anover-Sombke
Sanja Ugrinovic
Dinakantha S Kumararatne
Tatiana C Lawrence
E Michael Gertz
H Bobby Gaspar

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