Lysosomal Storage Disease in Iran (Report of Molecular Study)

نویسندگان
Massoud HOUSHMAND ID 1
Seyed Hassan TONEKABONI ID 2
Parvaneh KARIMZADEH ID 3
Omid ARYANi ID 4
Mohammad Reza ALAEE ID 5
Shahla FARSHIDI ID 6
Mahmoudreza ASHRAFI ID 7
Shadab SALEHPOUR ID 8
Shervin BADV ID 9
Marjan SHAKIBA ID 10

1 1. Assistant Professor of Human Molecular Genetics, Department of Medical Genetic, National Institute for Genetic Engineering and Biotechnology, Tehran, Iran

2 2.Professor of Pediatric Neurology, Pediatric Neurology Research Center, Shahid Beheshti University of Medical sciences,Tehran, Iran

3 Professor of Pediatric Neurology, Pediatric Neurology Research Center, Shahid Beheshti University of Medical sciences,Tehran, Iran

4 Genetic Counselor, Medical Genetic Dep. Special Medical Center, Tehran, Iran

5 Associate Professor of Endocrinology, Shahid Beheshti University of Medical Sciences (SBMU), Tehran, Iran

6 Nasle Omid Hope Foundation

7 Professor of Pediatric Neurology, Growth and Development Research Center, Children´s Medical Center, Tehran University of Medical Science, Tehran, Iran

8 Associate Professor of Pediatric Endocrinology and Metabolism, Shahid Beheshti University of Medical Sciences, Tehran, Iran

9 Assistant Professor of Pediatric Neurology, Zanjan University of Medical Sciences, Zanjan, Iran

10 Associate Professor of Pediatric Endocrinology and Metabolism, Shahid Beheshti University of Medical Sciences, Tehran, Iran

doi
10.22037/ijcn.v6i4.3908
چکیده

How to Cite this Article: Houshmand M, Tonekaboni SH, Karimzadeh P, Aryani O, AshrafiMR, Salehpour Sh, Badv Sh, Shakiba M, Alaee MR, Farshid Sh. Lysosomal Storage Disease inIran. (Report of Molecular Study). Iran J Child Neurol Autumn 2012; 6:4 (suppl. 1): 22. Pls see PDF.

کلیدواژه‌ها
Genetic, lysosomal storage disease, Child, Iran