Early and late manifestations of neuropathy due to HSPB1 mutation in the Jewish Iranian population-Reference-Cited by-同舟云学术

Early and late manifestations of neuropathy due to HSPB1 mutation in the Jewish Iranian population

Published:2021-05-11 Issue:6 Volume:8 Page:1260-1268
ISSN:2328-9503
Container-title:Annals of Clinical and Translational Neurology
language:en
Short-container-title:Ann Clin Transl Neurol

Author:

Greenbaum Lior¹²³^ORCID,Ben‐David Merav⁴,Nikitin Vera⁴,Gera Orna³⁴,Barel Ortal⁵⁶,Hersalis‐Eldar Adi⁴,Shamash Jana¹,Shimshoviz Noam⁵⁶,Reznik‐Wolf Haike¹,Shohat Mordechai³⁵⁶,Dominissini Dan³⁵⁶,Pras Elon¹³,Dori Amir³⁴^ORCID

Affiliation:

1. The Danek Gertner Institute of Human Genetics Sheba Medical Center Tel Hashomer Israel

2. The Joseph Sagol Neuroscience Center Sheba Medical Center Tel Hashomer Israel

3. Sackler Faculty of Medicine Tel Aviv University Tel Aviv Israel

4. Department of Neurology Sheba Medical Center Tel Hashomer Israel

5. The Genomic Unit Sheba Cancer Research Center, Sheba Medical Center Tel Hashomer Israel

6. Wohl Institute of Translational Medicine Sheba Medical Center Tel Hashomer Israel

Publisher

Wiley

Subject

Clinical Neurology,General Neuroscience

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/acn3.51362

Reference25 articles.

1. Charcot-Marie-Tooth 2F (Hsp27 mutations): A review

2. A novel HSPB1 mutation associated with a late onset CMT2 phenotype: Case presentation and systematic review of the literature

3. Mutations in HspB1 and hereditary neuropathies

4. Heat shock protein 27 R127W mutation: evidence of a continuum between axonal Charcot-Marie-Tooth and distal hereditary motor neuropathy

5. Axonal Neuropathies due to Mutations in Small Heat Shock Proteins: Clinical, Genetic, and Functional Insights into Novel Mutations

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