Causative variants linked with limb girdle muscular dystrophy in an Iranian population: 6 novel variants

Author:

Mianesaz Hamidreza12ORCID,Ghalamkari Safoura23,Salehi Mansoor24,Behnam Mahdiyeh45,Hosseinzadeh Majid26,Basiri Keivan78,Ghasemi Majid78,Sedghi Maryam67,Ansari Behnaz89

Affiliation:

1. Department of Human Genetics, Medical School University of Debrecen Debrecen Hungary

2. Department of Genetics and Molecular Biology Isfahan University of Medical Sciences Isfahan Iran

3. Division of Clinical Genetics, Department of Laboratory Medicine, Faculty of Medicine University of Debrecen Debrecen Hungary

4. Cellular, Molecular and Genetics Research Center Isfahan University of Medical Sciences Isfahan Iran

5. Student Research Committee Semnan University of Medical Science Semnan Iran

6. Medical Genetics Laboratory, Alzahra University Hospital Isfahan University of Medical Sciences Isfahan Iran

7. Metabolic Disorders Research Center, Endocrinology and Metabolism Molecular‐Cellular Sciences Institute Tehran University of Medical Science Tehran Iran

8. Department of Neurology Isfahan University of Medical Sciences Isfahan Iran

9. Isfahan Neuroscience Research Center, ALzahra Research Institute Isfahan University of Medical Science Isfahan Iran

Funder

Isfahan University of Medical Sciences

Publisher

Wiley

Subject

Genetics (clinical),Genetics,Molecular Biology

Reference59 articles.

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2. A simplified laminin nomenclature

3. The first case of primary alpha‐sarcoglycanopathy identified in Albania, in two siblings with homozygous alpha‐sarcoglycan mutation;Babameto‐Laku A.;Genetic Counseling,2011

4. Beta‐sarcoglycan gene mutations in Turkey;Balci B.;Acta Myologica: Myopathies and Cardiomyopathies: Official Journal of the Mediterranean Society of Myology,2004

5. A gene related to Caenorhabditis elegans spermatogenesis factor fer-1 is mutated in limb-girdle muscular dystrophy type 2B

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