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CCDC22
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Missense variant in CCDC22 causes X-linked recessive intellectual disability with features of Ritsch…
Commander Complex-A Multifaceted Operator in Intracellular Signaling and Cargo.
Hemizygous variants in protein phosphatase 1 regulatory subunit 3F (PPP1R3F) are associated with a n…
Expanding the pre- and postnatal phenotype of WASHC5 and CCDC22 -related Ritscher-Schinzel syndromes…
CCDC22 deficiency in humans blunts activation of proinflammatory NF-κB signaling.
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