FIELD: biotechnology.
SUBSTANCE: invention refers to biotechnology, namely to molecular biology, medical genetics and otorhinolaryngology. Disclosed are synthetic oligonucleotides for diagnosing (genotyping) of 35delG (rs80338939) mutation of GJB2 gene in human biomaterial. Primers are combined into kits for detecting DNA in blood and other biological materials by polymerase chain reaction.
EFFECT: invention enables highly sensitive diagnosis of congenital hereditary deafness in biological material; using this method provides also highly sensitive and objective description of human genotype with determination of homozygous and heterozygous carriage of this mutation.
1 cl, 2 dwg, 2 tbl
Title | Year | Author | Number |
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DIAGNOSTIC TECHNIQUE FOR THE 167DELT (RS80338942) MUTATION OF THE GJB2 GENE | 2020 |
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METHOD OF DNA-DIAGNOSTICS OF AUTOSOMAL RECESSIVE DEAFNESS-103 | 2019 |
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Authors
Dates
2020-12-29—Published
2020-04-22—Filed