Zobrazeno 1 - 4
of 4
pro vyhledávání: '"E R, Grinberg"'
Publikováno v:
Molecular Biology. 41:677-679
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::396481140a3796e217d363d865098d24
https://doi.org/10.1134/s0026893307040243
https://doi.org/10.1134/s0026893307040243
Autor:
L U, Dzhemileva, E R, Grinberg, A M, Tazetdinov, I S, Zaĭĭdullin, M M, Bibkov, V V, Musina, E K, Khusnutdinova
Publikováno v:
Molekuliarnaia biologiia. 42(1)
The review on problem tapetoretinal degeneration (TD) which represents serious enough and incurable disease revealed with frequency 1 : 3500-5000 in general population is presented. The most often reason of occurrence TD are mutations in RHO, RDS and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f14aafa830d73dc02272ab529309d3c6
https://pubmed.ncbi.nlm.nih.gov/18389614
https://pubmed.ncbi.nlm.nih.gov/18389614
Publikováno v:
Molekuliarnaia biologiia. 41(4)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::35404651696378fc516d960a337a7802
https://pubmed.ncbi.nlm.nih.gov/17936999
https://pubmed.ncbi.nlm.nih.gov/17936999
Publikováno v:
Vestnik otorinolaringologii. (4)
Congenital deafness is a severe, incurable and hardly correctable inherited disease. Mutations in GCB2 and GJB6 genes are most prevalent causes of deafness and occur in patients with hereditary and sporadic deafness all over the world. Some ethnic gr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f6c6ca42f4d4529077fdf6146c42c268
https://pubmed.ncbi.nlm.nih.gov/17152467
https://pubmed.ncbi.nlm.nih.gov/17152467