FIELD: medicine; otorhinolaryngology.
SUBSTANCE: new method of definition of mutations of gene MTRNR1 is offered. The invention can be used for diagnostics of acute forms of perceptive hearing loss.
EFFECT: reduction of research time.
2 dwg, 1 tbl, 2 ex
| Title | Year | Author | Number |
|---|---|---|---|
| METHOD OF DETECTING MUTATIONS IN GENE MYO7A, ACCOMPANIED BY DEVELOPMENT OF NON-SYNDROMIC AUTOSOMAL RECESSIVE DEAFNESS AND USHER SYNDROME | 2013 |
|
RU2555755C1 |
| METHOD FOR DETECTING 17 GJB2 AND GJB6 GENE MUTATIONS ACCOMPANYING NONSYNDROMIC DEAFNESS | 2010 |
|
RU2448163C2 |
| METHOD FOR REVEALING c-53-2A>G MUTATION IN PRESTIN GENE (SLC26A5) CAUSING DEVELOPMENT OF NON-SYNDROME-BASED AUTSOMAL-RECESSIVE DEAFNESS | 2012 |
|
RU2505608C1 |
| METHOD FOR DETECTION OF MUTATIONS INGJB2 GENE ACCOMPANYING WITH DEVELOPMENT OF NONSYNDROMAL AUTOSOMAL-RECESSIVE DEAFNESS | 2006 |
|
RU2317547C1 |
| DIAGNOSTIC TECHNIQUE FOR THE 167DELT (RS80338942) MUTATION OF THE GJB2 GENE | 2020 |
|
RU2739943C1 |
| METHOD FOR DIFFERENTIAL AND CONFIRMING MOLECULAR GENETIC DIAGNOSIS OF SENSORINEURAL HEARING LOSS IN A POPULATION OF CHUVASH | 2021 |
|
RU2768033C1 |
| METHOD OF DNA-DIAGNOSTICS OF AUTOSOMAL RECESSIVE DEAFNESS-103 | 2019 |
|
RU2727684C1 |
| DIAGNOSTIC TECHNIQUE OF 35DELG (RS80338939) MUTATION OF GJB2 GENE | 2020 |
|
RU2739889C1 |
| METHOD FOR DIAGNOSING MUTATION C.-23+1G>A (RS80338940) OF THE GJB2 GENE | 2020 |
|
RU2746055C1 |
| METHOD OF DETECTING MUTATIONS OF GJB2 GENE CAUSING AUTOSOMAL-RECESSIVE DEAFNESS 1A TYPE | 2017 |
|
RU2688180C1 |
