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Year | Number of Results |
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2022 | 4 |
2023 | 2 |
2024 | 1 |
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aysylumurtazina
(1 results)?
The First Russian Patient with Native American Myopathy.
Genes (Basel). 2022 Feb 13;13(2):341. doi: 10.3390/genes13020341.
Genes (Basel). 2022.
PMID: 35205385
Free PMC article.
Genetic and Clinical Spectrum of GNE Myopathy in Russia.
Murtazina A, Nikitin S, Rudenskaya G, Sharkova I, Borovikov A, Sparber P, Shchagina O, Chukhrova A, Ryzhkova O, Shatokhina O, Orlova A, Udalova V, Kanivets I, Korostelev S, Polyakov A, Dadali E, Kutsev S.
Murtazina A, et al.
Genes (Basel). 2022 Oct 31;13(11):1991. doi: 10.3390/genes13111991.
Genes (Basel). 2022.
PMID: 36360228
Free PMC article.
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Expanding the Phenotype of Hereditary Congenital Facial Paresis Type 3.
Murtazina A, Borovikov A, Kuchina A, Ovsova O, Bulakh M, Chukhrova A, Braslavskaya S, Ryzhkova O, Skryabin N, Kutsev S, Dadali E.
Murtazina A, et al.
Int J Mol Sci. 2023 Dec 21;25(1):129. doi: 10.3390/ijms25010129.
Int J Mol Sci. 2023.
PMID: 38203298
Free PMC article.
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Congenital myopathy as a new phenotype caused by two undescribed variants in ASCC1 gene.
Sharova M, Guseva D, Kurenkov A, Novoselova O, Murtazina A, Skoblov M.
Sharova M, et al. Among authors: murtazina a.
Am J Med Genet A. 2022 Oct;188(10):3100-3105. doi: 10.1002/ajmg.a.62898. Epub 2022 Jul 15.
Am J Med Genet A. 2022.
PMID: 35838082
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The Presentation of Two Unrelated Clinical Cases from the Republic of North Ossetia-Alania with the Same Previously Undescribed Variant in the COL6A2 Gene.
Ionova SA, Murtazina AF, Tebieva IS, Getoeva ZK, Dadali EL, Chausova PA, Shchagina OA, Marakhonov AV, Kutsev SI, Zinchenko RA.
Ionova SA, et al. Among authors: murtazina af.
Int J Mol Sci. 2022 Oct 12;23(20):12127. doi: 10.3390/ijms232012127.
Int J Mol Sci. 2022.
PMID: 36292982
Free PMC article.
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Mild phenotype of CHAT-associated congenital myasthenic syndrome: case series.
Murtazina A, Borovikov A, Marakhonov A, Sharkov A, Sharkova I, Mirzoyan A, Kulikova S, Ganieva R, Zabnenkova V, Ryzhkova O, Nikitin S, Dadali E, Kutsev S.
Murtazina A, et al.
Front Pediatr. 2024 Jan 18;12:1280394. doi: 10.3389/fped.2024.1280394. eCollection 2024.
Front Pediatr. 2024.
PMID: 38304750
Free PMC article.
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X-Linked Myotubular Myopathy in a Female Patient with a Pathogenic Variant in the MTM1 Gene.
Chausova P, Murtazina A, Stepanova A, Borovicov A, Kovalskaia V, Ryadninskaya N, Chukhrova A, Ryzhkova O, Poliakov A.
Chausova P, et al. Among authors: murtazina a.
Int J Mol Sci. 2023 May 7;24(9):8409. doi: 10.3390/ijms24098409.
Int J Mol Sci. 2023.
PMID: 37176116
Free PMC article.
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