Common variable immunodeficiency in two kindreds with heterogeneous phenotypes caused by novel heterozygous NFKB1 mutations #HelsinkiHealth #tutkimus #tiede https://t.co/MqRp0aGDeD
1,238 followers
321 followers
Common variable immunodeficiency in two kindreds with heterogeneous phenotypes caused by novel heterozygous NFKB1 mutations https://t.co/dHLPViv00P
321 followers
Common variable immunodeficiency in two kindreds with heterogeneous phenotypes caused by novel heterozygous NFKB1 mutations https://t.co/gZpZjis9WW https://t.co/XdFHJJnyAd
721 followers
RT @Primary_Immune: "...2 families with novel heterozygous 🧬NFKB1 mutations and diverging phenotypes ranging from CVID with infectious susc…