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maria sumita
(6 results)?
Leigh Syndrome: Spectrum of Molecular Defects and Clinical Features in Russia.
Int J Mol Sci. 2023 Jan 13;24(2):1597. doi: 10.3390/ijms24021597.
Int J Mol Sci. 2023.
PMID: 36675121
Free PMC article.
Rare IFT140-Associated Phenotype of Cranioectodermal Dysplasia and Features of Diagnostic Journey in Patients with Suspected Ciliopathies.
Sharova M, Markova T, Sumina M, Petukhova M, Bulakh M, Ryzhkova O, Nagornova T, Ionova S, Marakhonov A, Dadali E, Kutsev S.
Sharova M, et al. Among authors: sumina m.
Genes (Basel). 2023 Jul 28;14(8):1553. doi: 10.3390/genes14081553.
Genes (Basel). 2023.
PMID: 37628605
Free PMC article.
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Clinical and Genetic Characteristics of Calvarial Doughnut Lesions with Bone Fragility in Three Families with a Reccurent SGMS2 Gene Variant.
Merkuryeva E, Markova T, Tyurin A, Valeeva D, Kenis V, Sumina M, Sorokin I, Shchagina O, Skoblov M, Nefedova M, Khusainova R, Zakharova E, Dadali E, Kutsev S.
Merkuryeva E, et al. Among authors: sumina m.
Int J Mol Sci. 2023 Apr 28;24(9):8021. doi: 10.3390/ijms24098021.
Int J Mol Sci. 2023.
PMID: 37175737
Free PMC article.
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