LEUKOCYTE DISORDERS

Mutations in the lamin B-receptor gene.

Mutation in the MYH9 gene.

Mutation in the CHS1 LYST gene.

Abnormal random and chemotactic movement.

Normal random movement, abnormal chemotactic movement.

Mutation in the ITGB2 gene.

Mutation in the SLC35C1 gene.

Mutation in the Kindlin-3 protein.

CXCR4 mutation

NADPH oxidase defiency.

Beta-glucocerebrosidase deficiency.

Acid sphingomyelinase deficiency.

BTK deficiency.

TBX1 gene

IL2RG gene mutation

WASp protein deficiency.