The Frequency of DYT1 (GAG Deletion) Mutation in Primary Dystonia Patients from Iran
In: Cell Journal, Jg. 13 (2011), Heft 1, S. 55-58
Online
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Zugriff:
Objective: To determine the frequency of DYT1 mutation in Iranian patients affected withprimary dystonia.Materials and Methods: In this study, we investigated 60 patients with primary dystoniawho referred to the Tehran Medical Genetics Laboratory (TMGL) to determine thedeletional mutation of 904-906 del GAG in the DYT1 gene. DNA extracted from patients’peripheral blood was subjected to PCR-sequencing for exon 5 of the DYT1 gene. The collectionof samples was based on random sampling.Results: The deletional mutation of 904-906 del GAG in the DYT1 gene (15099 to 15101based on reference sequence: NG_008049.1) was identified in 11 patients (18.33%). Theaverage age of affected patients with this mutation was 13.64 ± 7.4 years.Conclusion: It can be concluded that the DYT1 deletional mutation of 904-906 del GAGhas a high frequency in Iranian patients in comparison with other non-Jewish populations.Therefore, this particular mutation may be the main representative of pathogenic DYT1gene for a large proportion of Iranian patients with primary dystonia.
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The Frequency of DYT1 (GAG Deletion) Mutation in Primary Dystonia Patients from Iran
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Autor/in / Beteiligte Person: | Hamid, Mohammad ; Zand, Zahra ; Gholam Ali Shahidi ; Mohammad Taghi Akbari |
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Zeitschrift: | Cell Journal, Jg. 13 (2011), Heft 1, S. 55-58 |
Veröffentlichung: | Royan Institute (ACECR), Tehran, 2011 |
Medientyp: | academicJournal |
ISSN: | 2228-5806 (print) ; 2228-5814 (print) |
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