Identifying Novel Mutations in Iranian Patients with LPS-responsive Beige-like Anchor Protein (LRBA) Deficiency

Author:

Ghaini Mehdi1,Arzanian Mohammad Taghi2,Shamsian Bibi Shahin2,Sadr Saeed3,Rohani Pejman4,Keramatipour Mohammad5,Mesdaghi Mehrnaz1,Eskandarzadeh Shabnam1,Lo Bernice6,Jamee Mahnaz78,Chavoshzadeh Zahra1

Affiliation:

1. Immunology and Allergy Department, Mofid Children’s Hospital, Shahid Beheshti University of Medical Science, Tehran, Iran

2. Department of Pediatric Hematology and Oncology, Mofid Children’s Hospital, Shahid Beheshti University of Medical Science, Tehran, Iran

3. Department of Pediatric Pulmonology, Mofid Children’s Hospital, Shahid Beheshti University of Medical Science, Tehran, Iran

4. Department of Pediatric Gastroenterology and Hepatology, Mofid Children’s Hospital, Shahid Beheshti University of Medical Sciences, Tehran, Iran

5. Department of Medical Genetics, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran

6. Department of Human Genetics, Research Branch, Sidra Medicine, Doha, Qatar

7. Student Research Committee, Alborz University of Medical Sciences, Karaj, Iran

8. Alborz Office of USERN, Universal Scientific Education and Research Network (USERN), Alborz University of Medical Sciences, Karaj, Iran

Publisher

Informa UK Limited

Subject

General Medicine,Immunology

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