Crossref

1. Phenotypic intrafamilial variability including H syndrome and Rosai–Dorfman disease associated with the same c.1088G > A mutation in the SLC29A3 gene

- Hamza Chouk

- Mohamed Ben Rejeb

- Lobna Boussofara

- Haїfa Elmabrouk

- Najet Ghariani

- Badreddine Sriha

- Ali Saad

- Dorra H’Mida

- Mohamed Denguezli

2. Review of the current literature on H syndrome treatment

- Kimia Saleh Anaraki

- Sepehr Khosravi

- Elham Behrangi

- Afsaneh Sadeghzadeh-Bazargan

- Azadeh Goodarzi

3. Mycophenolate mofetil treatment of an H syndrome patient with a SLC29A3 mutation

- Elham Behrangi

- Afsaneh Sadeghzadeh‐Bazargan

- Sepehr Khosravi

- Mahsa Shemshadi

- Leila Youssefian

- Hassan Vahidnezhad

- Azadeh Goodarzi

- Jouni Uitto

4. Identification of a novel homozygous frameshift mutation in SLC29A3 gene in a case with H syndrome from Iran

- Rita Bagherian

- Farideh Yousefipour

- Houriyeh Sadat Mousavi

- Fatemeh Saffari

- Elham HajiShafieha

- Samin Nesbat Mohammadi

- Hadi Mousakhani

- Seyed Mohammad Fathi

- Amirhossein Mehrtash

- Fatemeh Masomi Verki

- Donghyun Lee

- Abolfazl Heidari