Description of combined ARHSP/JALS phenotype in some patients with SPG11 mutations-Reference-Cited by-同舟云学术

Description of combined ARHSP/JALS phenotype in some patients with SPG11 mutations

Published:2020-05-08 Issue:7 Volume:8 Page:
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Mol Genet Genomic Med

Author:

Khani Marzieh¹,Shamshiri Hosein²,Fatehi Farzad²,Rohani Mohammad³,Haghi Ashtiani Bahram⁴,Akhoundi Fahimeh Haji⁴,Alavi Afagh⁵^ORCID,Moazzeni Hamidreza¹,Taheri Hanieh¹,Ghani Mina Tolou¹,Javanparast Leila⁵,Hashemi Seyyed Saleh⁵,Haji‐Seyed‐Javadi Ramona⁶,Heidari Matineh⁴,Nafissi Shahriar²,Elahi Elahe¹^ORCID

Affiliation:

1. School of Biology College of Science University of Tehran Tehran Iran

2. Department of Neurology Shariati Hospital, Tehran University of Medical Sciences Tehran Iran

3. Department of Neurology Hazrat Rasool HospitalIran University of Medical Sciences Tehran Iran

4. Department of Neurology Firoozgar HospitalIran University of Medical Sciences Tehran Iran

5. Genetics Research Center University of Social Welfare and Rehabilitation Sciences Tehran Iran

6. Department of Radiation Oncology Emory University School of Medicine Atlanta GA USA

Publisher

Wiley

Subject

Genetics(clinical),Genetics,Molecular Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.1240

Reference55 articles.

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2. Genetic analysis and SOD1 mutation screening in Iranian amyotrophic lateral sclerosis patients

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4. A teljesexom-szekvenálás jelentősége a ritka neurológiai betegségek diagnosztikájában – saját tapasztalatok egy ataxiás eset kapcsán

5. Complex genomic rearrangement in SPG11 due to a DNA replication-based mechanism

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