Table of Contents



Washington University Experience | MISCELLANEOUS | Familial erythrophagic lymphohistiocytosis | 3F3 HLH, Perforin1 mutation (Case 3) NF 3

3F3 HLH, Perforin1 mutation (Case 3) NF 3
Axons are well maintained (NF IHC)



Gallery RSS RSS Feed | Archive View | Login | Powered by Zenphoto