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Autoimmune polyglandular syndrome type 1 in Russian patients: clinical variants and autoimmune regulator mutations.
Horm Res Paediatr. 2010;73(6):449-57. doi: 10.1159/000313585. Epub 2010 Apr 20.
Horm Res Paediatr. 2010.
PMID: 20407228
Four Novel Disease-Causing Variants in the NOTCH3 Gene in Russian Patients with CADASIL.
Bostanova F, Tsygankova P, Nagornov I, Dadali E, Bessonova L, Kulesh A, Drobakha V, Danchenko I, Kanivets I, Zakharova E.
Bostanova F, et al.
Genes (Basel). 2023 Aug 28;14(9):1715. doi: 10.3390/genes14091715.
Genes (Basel). 2023.
PMID: 37761855
Free PMC article.
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TNF gene polymorphisms in cystic fibrosis patients: contribution to the disease progression.
Shmarina G, Pukhalsky A, Petrova N, Zakharova E, Avakian L, Kapranov N, Alioshkin V.
Shmarina G, et al.
J Transl Med. 2013 Jan 23;11:19. doi: 10.1186/1479-5876-11-19.
J Transl Med. 2013.
PMID: 23343370
Free PMC article.
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Does the c.-14C>T Mutation in the IFITM5 Gene Provide Identical Phenotypes for Osteogenesis Imperfecta Type V? Data from Russia and a Literature Review.
Tyurin A, Merkuryeva E, Zaripova A, Markova T, Nagornova T, Dantsev I, Nadyrshina D, Zakharova E, Khusainova R.
Tyurin A, et al.
Biomedicines. 2022 Sep 22;10(10):2363. doi: 10.3390/biomedicines10102363.
Biomedicines. 2022.
PMID: 36289625
Free PMC article.
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