The first report of two homozygous sequence variants in FKRP and SELENON genes associated with syndromic congenital muscular dystrophy in Iran: Further expansion of the clinical phenotypes-Reference-Cited by-同舟云学术

The first report of two homozygous sequence variants in FKRP and SELENON genes associated with syndromic congenital muscular dystrophy in Iran: Further expansion of the clinical phenotypes

Published:2020-09-29 Issue:12 Volume:22 Page:
ISSN:1099-498X
Container-title:The Journal of Gene Medicine
language:en
Short-container-title:J Gene Med

Author:

Mohamadian Malihe¹^ORCID,Naseri Mohsen²^ORCID,Ghandil Pegah³⁴^ORCID,Bahrami Afsane²,Momen Ali Akbar⁵

Affiliation:

1. Department of Molecular Medicine Birjand University of Medical Sciences Birjand Iran

2. Cellular and Molecular Research Center Birjand University of Medical Sciences Birjand Iran

3. Diabetes Research Center, Health Research Institute Ahvaz Jundishapur University of Medical Sciences Ahvaz Iran

4. Department of Medical Genetics, School of Medicine Ahvaz Jundishapur University of Medical Sciences Ahvaz Iran

5. Department of Paediatric Neurology, Golestan Medical, Educational, and Research Center Ahvaz Jundishapur University of Medical Sciences Ahvaz Iran

Publisher

Wiley

Subject

Genetics(clinical),Drug Discovery,Genetics,Molecular Biology,Molecular Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/jgm.3265

Reference36 articles.

1. Congenital muscular dystrophy. Part I: a review of phenotypical and diagnostic aspects

2. Congenital muscular dystrophy. Part II: a review of pathogenesis and therapeutic perspectives

3. Muscular Dystrophies

4. Muscular Dystrophies and Other Genetic Myopathies

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