Tinsa_2019_J.Pediatr.Hematol.Oncol_41_e193

Reference

Title : A Novel Mutation c.153 C>A in a Tunisian Girl With Wolman Disease and Unusual Presentation: Hemophagocytic Lymphohistiocytosis - Tinsa_2019_J.Pediatr.Hematol.Oncol_41_e193
Author(s) : Tinsa F , Ben Romdhane M , Boudabous H , Bel Hadj I , Brini I , Tebib N , Louati H , Bekri S , Boussetta K
Ref : J Pediatr Hematol Oncol , 41 :e193 , 2019
Abstract : Tinsa_2019_J.Pediatr.Hematol.Oncol_41_e193
ESTHER : Tinsa_2019_J.Pediatr.Hematol.Oncol_41_e193
PubMedSearch : Tinsa_2019_J.Pediatr.Hematol.Oncol_41_e193
PubMedID: 29702543
Gene_locus related to this paper: human-LIPA

Related information

Gene_locus related to this paper: human-LIPA

Citations formats

Tinsa F, Ben Romdhane M, Boudabous H, Bel Hadj I, Brini I, Tebib N, Louati H, Bekri S, Boussetta K (2019)
A Novel Mutation c.153 C>A in a Tunisian Girl With Wolman Disease and Unusual Presentation: Hemophagocytic Lymphohistiocytosis
J Pediatr Hematol Oncol 41 :e193

Tinsa F, Ben Romdhane M, Boudabous H, Bel Hadj I, Brini I, Tebib N, Louati H, Bekri S, Boussetta K (2019)
J Pediatr Hematol Oncol 41 :e193