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Case Report: A Novel Homozygous Variant of the SERPINF1 Gene in Rare Osteogenesis Imperfecta Type VI.
Int J Mol Sci. 2023 Apr 3;24(7):6672. doi: 10.3390/ijms24076672.
Int J Mol Sci. 2023.
PMID: 37047644
Free PMC article.
Application of Long-Read Nanopore Sequencing to the Search for Mutations in Hypertrophic Cardiomyopathy.
Salakhov RR, Golubenko MV, Valiakhmetov NR, Pavlyukova EN, Zarubin AA, Babushkina NP, Kucher AN, Sleptcov AA, Nazarenko MS.
Salakhov RR, et al. Among authors: valiakhmetov nr.
Int J Mol Sci. 2022 Dec 13;23(24):15845. doi: 10.3390/ijms232415845.
Int J Mol Sci. 2022.
PMID: 36555486
Free PMC article.
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