Angiogenin mutations in Hungarian patients with amyotrophic lateral sclerosis: Clinical, genetic, computational, and functional analyses-Reference-Cited by-同舟云学术

Angiogenin mutations in Hungarian patients with amyotrophic lateral sclerosis: Clinical, genetic, computational, and functional analyses

Published:2019-04-25 Issue:6 Volume:9 Page:
ISSN:2162-3279
Container-title:Brain and Behavior
language:en
Short-container-title:Brain Behav

Author:

Tripolszki Kornélia¹^ORCID,Danis Judit²,Padhi Aditya K.³,Gomes James³,Bozó Renáta⁴,Nagy Zsófia F.¹,Nagy Dóra¹,Klivényi Péter⁵,Engelhardt József I.⁵,Széll Márta¹²

Affiliation:

1. Department of Medical Genetics University of Szeged Szeged Hungary

2. MTA‐SZTE Dermatological Research Group Szeged Hungary

3. Kusuma School of Biological Sciences Indian Institute of Technology Delhi New Delhi India

4. Department of Dermatology and Allergology University of Szeged Szeged Hungary

5. Department of Neurology University of Szeged Szeged Hungary

Funder

Hungarian Brain Research Program

Publisher

Wiley

Subject

Behavioral Neuroscience

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/brb3.1293

Reference40 articles.

1. ALSoD: A user-friendly online bioinformatics tool for amyotrophic lateral sclerosis genetics

2. Structural insights into human angiogenin variants implicated in Parkinson’s disease and Amyotrophic Lateral Sclerosis

3. A novel Angiogenin gene mutation in a sporadic patient with amyotrophic lateral sclerosis from southern Italy

4. Identification of novel Angiogenin (ANG) gene missense variants in German patients with amyotrophic lateral sclerosis

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