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Corrigendum: Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A.
Published in:
2004
By:
- Züchner, S;
- Mersiyanova, I V;
- Muglia, M;
- Bissar-Tadmouri, N;
- Rochelle, J;
- Dadali, E L;
- Zappia, M;
- Nelis, E;
- Patitucci, A;
- Senderek, J;
- Parman, Y;
- Evgrafov, O;
- Jonghe, P De;
- Takahashi, Y;
- Tsuji, S;
- Pericak-Vance, M A;
- Quattrone, A;
- Battologlu, E;
- Polyakov, A V;
- Timmerman, V
Publication type:
Correction Notice
KIF1A-related autosomal dominant spastic paraplegias (SPG30) in Russian families.
Published in:
2020
By:
- Rudenskaya, G. E.;
- Kadnikova, V. A.;
- Ryzhkova, O. P.;
- Bessonova, L. A.;
- Dadali, E. L.;
- Guseva, D. S.;
- Markova, T. V.;
- Khmelkova, D. N.;
- Polyakov, A. V.
Publication type:
journal article
HINT1 gene pathogenic variants: the most common cause of recessive hereditary motor and sensory neuropathies in Russian patients.
Published in:
Molecular Biology Reports, 2020, v. 47, n. 2, p. 1331, doi. 10.1007/s11033-019-05238-z
By:
- Shchagina, O. A.;
- Milovidova, T. B.;
- Murtazina, A. F.;
- Rudenskaya, G. E.;
- Nikitin, S. S.;
- Dadali, E. L.;
- Polyakov, A. V.
Publication type:
Article
Clinical and Genetic Characteristics of Noonan Syndrome and Noonan-like Diseases.
Published in:
Russian Journal of Genetics, 2020, v. 56, n. 5, p. 540, doi. 10.1134/S1022795420050117
By:
- Orlova, A. A.;
- Dadali, E. L.;
- Polyakov, A. V.
Publication type:
Article
Clinical Population Genetics of Hereditary Diseases among Children of the Karachay-Cherkess Republic.
Published in:
Russian Journal of Genetics, 2019, v. 55, n. 8, p. 1033, doi. 10.1134/S1022795419080180
By:
- Zinchenko, R. A.;
- Kadyshev, V. V.;
- Galkina, V. A.;
- Dadali, E. L.;
- Mikhailova, L. K.;
- Marakhonov, A. V.;
- Petrova, N. V.;
- Petrina, N. E.;
- El'chinova, G. I.;
- Alexandrova, O. Yu.;
- Kutsev, S. I.;
- Ginter, E. K.
Publication type:
Article
Molecular and Genetic Study of Limb-Girdle Muscular Dystrophy 2D in Patient Cohorts with Various Forms of Progressive Muscular Dystrophies.
Published in:
Russian Journal of Genetics, 2019, v. 55, n. 2, p. 238, doi. 10.1134/S1022795419020030
By:
- Bulakh, M. V.;
- Galeeva, N. M.;
- Polyakova, D. A.;
- Ryzhkova, O. P.;
- Dadali, E. L.;
- Polyakov, A. V.
Publication type:
Article
Diversity and Prevalence of Hereditary Diseases among Nogais of the Karachay-Cherkess Republic.
Published in:
Russian Journal of Genetics, 2018, v. 54, n. 7, p. 858, doi. 10.1134/S1022795418070165
By:
- Zinchenko, R. A.;
- Makaov, A. Kh.;
- Kadyshev, V. V.;
- Galkina, V. A.;
- Dadali, E. L.;
- Mikhailova, L. K.;
- Shurygina, M. F.;
- Marakhonov, A. V.;
- Petrova, N. V.;
- Petrina, N. E.;
- El’chinonva, G. I.;
- Gundorova, P.;
- Tanas, A. S.;
- Strelnikov, V. V.;
- Polyakov, A. V.;
- Ginter, E. K.
Publication type:
Article
Medical Genetic Study of Hereditary Diseases in Abazins of the Karachay-Cherkess Republic.
Published in:
Russian Journal of Genetics, 2018, v. 54, n. 6, p. 703, doi. 10.1134/S1022795418060170
By:
- Zinchenko, R. A.;
- Makaov, A. Kh.;
- Kadyshev, V. V.;
- Galkina, V. A.;
- Dadali, E. L.;
- Shurygina, M. F.;
- El’chinova, G. I.;
- Mikhailova, L. K.;
- Marakhonov, A. V.;
- Vasilyeva, T. A.;
- Petrova, N. V.;
- Gundorova, P.;
- Tanas, A. S.;
- Strelnikov, V. V.;
- Polyakov, A. V.;
- Ginter, E. K.
Publication type:
Article
Genetic epidemiological study of Bashkortostan Republic: The effect of genetic structure of population on the load of monogenic hereditary diseases.
Published in:
Russian Journal of Genetics, 2009, v. 45, n. 4, p. 478, doi. 10.1134/S1022795409040139
By:
- Murzabaeva, S. Sh.;
- Zinchenko, R. A.;
- Greenberg, Ya. I.;
- Galkina, V. A.;
- Khlebnikova, O. V.;
- Dadali, E. L.;
- Fedotov, V. P.;
- El'chinova, G. I.;
- Terekhovskaia, I. G.;
- Khidiyatova, I. M.;
- Khusnutdinova, E. K.;
- Ginter, E. K.
Publication type:
Article
Genetic and Epidemiologic Analysis of Hereditary Diseases of the Nervous System in the Cities of Volgograd and Volzhsky.
Published in:
Russian Journal of Genetics, 2004, v. 40, n. 9, p. 1031, doi. 10.1023/B:RUGE.0000041383.57265.6b
By:
- Kirilenko, N. B.;
- Fedotov, V. P.;
- Baryshnikova, N. V.;
- Dadali, E. L.;
- Polyakov, A. V.;
- Zinchenko, R. A.
Publication type:
Article
Clinical Genetic Characteristics of Epilepsy Due to Mutations in the PCDH19 Gene (OMIM: 300088).
Published in:
Neuroscience & Behavioral Physiology, 2020, v. 50, n. 9, p. 1099, doi. 10.1007/s11055-020-01011-z
By:
- Dadali, E. L.;
- Mishina, I. A.;
- Borovikov, A. O.;
- Sharkov, A. A.;
- Kanivets, I. V.
Publication type:
Article

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