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Washington University Experience | MISCELLANEOUS | Familial erythrophagic lymphohistiocytosis | 3E2 HLH, Perforin1 mutation (Case 3) area A NF 10X
3E1,2 Adjacent sections stained for myelin (#3E1) and neurofilaments (#3E2) show modest loss of myelin with little evidence of axon loss in this section.
