Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Maria R, Lalayants"'
Autor:
Aisen V Solovyev, Alena Kushniarevich, Elena Bliznetz, Marita Bady-Khoo, Maria R Lalayants, Tatiana G Markova, Gabriel Minárik, L'udevít Kádasi, Ene Metspalu, Vera G Pshennikova, Fedor M Teryutin, Anatoly N Alekseev, Elza K Khusnutdinova, Alexander Poliakov, Mait Мetspalu, Olga L Posukh, Nikolay A Barashkov, Sardana A Fedorova
The mutations in the GJB2 gene are known to be a major cause of autosomal recessive deafness 1A (OMIM 220290). The most common pathogenic variants of the GJB2 gene have high ethno-geographic specificity in their distribution that being attributed to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1a1dcbfd6f9ec92417babfcf62bd10b3
https://doi.org/10.21203/rs.3.rs-670020/v1
https://doi.org/10.21203/rs.3.rs-670020/v1
Autor:
Aisen V, Solovyev, Alena, Kushniarevich, Elena, Bliznetz, Marita, Bady-Khoo, Maria R, Lalayants, Tatiana G, Markova, Gabriel, Minárik, L'udevít, Kádasi, Ene, Metspalu, Vera G, Pshennikova, Fedor M, Teryutin, Elza K, Khusnutdinova, Alexander, Poliakov, Mait, Metspalu, Olga L, Posukh, Nikolay A, Barashkov, Sardana A, Fedorova
Publikováno v:
Human genetics. 141(3-4)
Mutations in the GJB2 gene are known to be a major cause of autosomal recessive deafness 1A (OMIM 220290). The most common pathogenic variants of the GJB2 gene have a high ethno-geographic specificity in their distribution, being attributed to a foun
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::bc88e73c2c7d58e60dc50ee55370079b
https://pubmed.ncbi.nlm.nih.gov/34839402
https://pubmed.ncbi.nlm.nih.gov/34839402
