Spinal muscular atrophy carrier frequency in Ukraine

被引:0
|
作者
O. Soloviov
N. Hryschenko
L. Livshits
机构
[1] National Academy of Sciences of Ukraine,Department of Human Genomics, Institute of Molecular Biology and Genetics
来源
Russian Journal of Genetics | 2013年 / 49卷
关键词
Spinal Muscular Atrophy; Multiplex Ligation Dependent Probe Amplification; Survival Motor Neuron; Autosomal Recessive Disease; Ethnical Group;
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学科分类号
摘要
Background. Spinal muscular atrophy (SMA) is a common autosomal recessive neuromuscular disorder with the frequency of carriers in a number of ethnical groups ranging from 1/50 to 1/25. However, the prevalence of SMA for population of Ukraine remains to be established. Methods. For the analysis of deletion in exon 7 SMN1 gene in SYBR Green Real-Time qPCR assay specific for the single nucleotide change in exon 7 (c.840 C>T) was used. Results. Using SYBR Green qPCR assay, the incidence of the exon 7 SMN1 deletion was established among 370 unrelated individuals without family history of SMA. The carrier frequency for this group of Ukrainians was estimated as 3.24% (1/31). Conclusions. The results of our study showing the high prevalence of carriers warrant the importance of population screening for SMA in Ukraine.
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页码:982 / 983
页数:1
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