autosomal
characterised
defect
done
dysregulation
familial
families
fhl
haemophagocytic
harbour
harbouring
killer
leukaemia
lymphohistiocytosis
milder
mutational
myelogenous
nonsense
perforin
periods
prf1
psychomotor
recessive
retardation
segregation
syntaxin
uncommon
undertaken
unrelated
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