Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Vera N Tadinova"'
Autor:
Vera N Tadinova, S. N. Ponidelko, L. U. Dzhemilova, N. R. Maksimova, S. A. Fedorova, S. A. Zhuravskii, T. G. Markova, Nikolay A. Barashkov, Olga L. Posukh, E. K. Khusnutdinova, A. M. Tazetdinov
Publikováno v:
Russian Journal of Genetics. 45:861-869
Mitochondrial DNA (mtDNA) mutations play an important role in etiology of hereditary hearing loss. In various regions of the world, patients suffer from nonsyndromic sensorineural hearing loss initiated by aminoglycoside antibiotics. Mutations that h
Autor:
Rita Khusainova, I. A. Kutuev, Vera N Tadinova, I. M. Khidiyatova, Olga L. Posukh, Lilya U. Dzhemileva, S. A. Fedorova, Simeon L Lobov, V. L. Akhmetova, Nikolay A. Barashkov, Elza Khusnutdinova, I. R. Gilyazova
Publikováno v:
Journal of human genetics. 55(11)
Hearing impairment is one of the most common disorders of sensorineural function and the incidence of profound prelingual deafness is about 1 per 1000 at birth. GJB2 gene mutations make the largest contribution to hereditary hearing impairment. The s
Autor:
Nathalie Pallares-Ruiz, Ludmila P. Osipova, Anne-Françoise Roux, Olga L. Posukh, Mireille Claustres, Vera N Tadinova
Publikováno v:
BMC Medical Genetics
BMC Medical Genetics, Vol 6, Iss 1, p 12 (2005)
BMC Medical Genetics, Vol 6, Iss 1, p 12 (2005)
Background We studied the molecular basis of NSHL in Republic of Altai (South Siberia, Russia). The Altaians are the indigenous Asian population of the Altai Mountain region considered as a melting-pot and a dispersion center for world-wide human exp