A novel mutation in the ALS2 gene in an iranian kurdish family with juvenile amyotrophic lateral sclerosis-Reference-Cited by-同舟云学术

A novel mutation in the ALS2 gene in an iranian kurdish family with juvenile amyotrophic lateral sclerosis

Published:2022-07-19 Issue:1-2 Volume:24 Page:148-151
ISSN:2167-8421
Container-title:Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration
language:en
Short-container-title:Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration

Author:

Daneshmandpour Yousef¹²,Bahmanpour Zahra¹,Kazeminasab Somayeh¹^ORCID,Aghaei Moghadam Ehsan³,Alehabib Elham⁴,Chapi Marjan⁴,Tafakhori Abbas⁵,Aghaei Negar⁶,Darvish Hossein⁷⁸,Emamalizadeh Babak¹²^ORCID

Affiliation:

1. Department of Medical Genetics, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran

2. Cytogene Genetic Diagnostic Laboratory, Tabriz, Iran

3. Department of Pediatrics, School of Medicine, Children's Medical Center, Tehran University of Medical Sciences, Tehran, Iran

4. Student Research Committee, Shahid Beheshti University of Medical Sciences, Tehran, Iran

5. Iranian Center of Neurological Research, Neuroscience Institute, Tehran University of Medical Sciences, Tehran, Iran

6. Research Center of Psychiatry and Behavioral Sciences, Tabriz University of Medical Sciences, Tabriz, Iran

7. Neuroscience Research Center, Faculty of Medicine, Golestan University of Medical Sciences, Gorgan, Iran

8. Cancer Research Center, Semnan University of Medical Sciences, Semnan, Iran

Funder

Tabriz University of Sciences

Publisher

Informa UK Limited

Subject

Neurology (clinical),Neurology

Link

https://www.tandfonline.com/doi/pdf/10.1080/21678421.2022.2100263

Reference10 articles.

1. Novel mutation in theALS2 gene in juvenile amyotrophic lateral sclerosis

2. Alsin Is a Rab5 and Rac1 Guanine Nucleotide Exchange Factor

3. Variants in the ALS2 gene are not associated with sporadic amyotrophic lateral sclerosis

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