Genetic investigation of patients with autosomal recessive ataxia and identification of two novel variants in the SQSTM1 and SYNE1 genes.
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| Title: | Genetic investigation of patients with autosomal recessive ataxia and identification of two novel variants in the SQSTM1 and SYNE1 genes. |
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| Authors: | Mokhtari D; Department of Genetics and Pathology, Ardabil University of Medical Sciences, Ardabil, Iran., Jahanpanah M; Department of Genetics and Pathology, Ardabil University of Medical Sciences, Ardabil, Iran., Jabbari N; Department of Animal Biology, Faculty of Natural Science, University of Tabriz, Tabriz, Iran., Azari H; Department of Genetics and Pathology, Ardabil University of Medical Sciences, Ardabil, Iran., Davarnia S; Tabriz University of Medical Sciences, Tabriz, Iran., Mokaber H; Department of Biology, Ardabil Branch, Islamic Azad University, Ardabil, Iran., Arish S; Department of Genetics and Pathology, Ardabil University of Medical Sciences, Ardabil, Iran., Molatefi R; Department of Pediatrics, Bo-Ali Children's Hospital of Ardabil University of Medical Sciences, Ardabil, Iran.; Cancer Immunology and Immunotherapy Research Center, Ardabil University of Medical Sciences, Ardabil, Iran., Abbasi V; Department of Neurology, Ardabil University of Medical Sciences, Ardabil, Iran., Davarnia B; Department of Genetics and Pathology, Ardabil University of Medical Sciences, Ardabil, Iran. b.davarnia@gmail.com. |
| Source: | Human genome variation [Hum Genome Var] 2024 Aug 30; Vol. 11 (1), pp. 35. Date of Electronic Publication: 2024 Aug 30. |
| Publication Type: | Journal Article |
| Journal Info: | Publisher: Nature Publishing Group Country of Publication: England NLM ID: 101652445 Publication Model: Electronic Cited Medium: Print ISSN: 2054-345X (Print) Linking ISSN: 2054345X NLM ISO Abbreviation: Hum Genome Var Subsets: PubMed not MEDLINE |
| Database: | MEDLINE Ultimate |
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