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| Predominantly Antibody Deficiency v2.8 | Bryony Thompson Copied gene PRKCD from panel Common Variable Immunodeficiency | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Predominantly Antibody Deficiency v2.8 | PRKCD |
Bryony Thompson gene: PRKCD was added gene: PRKCD was added to Predominantly Antibody Deficiency. Sources: Expert Review Green,Melbourne Genomics Health Alliance Immunology Flagship,Victorian Clinical Genetics Services Mode of inheritance for gene: PRKCD was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: PRKCD were set to 23319571; 23666743; 23430113; 11976687; 33047643; 29867916 Phenotypes for gene: PRKCD were set to Autoimmune lymphoproliferative syndrome, type III, MIM# 615559; CVID 9 |
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