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Hemi- and Homozygous Loss-of-Function Mutations in DSG2 (Desmoglein-2) Cause Recessive Arrhythmogenic Cardiomyopathy with an Early Onset.
Int J Mol Sci. 2021 Apr 6;22(7):3786. doi: 10.3390/ijms22073786.
Int J Mol Sci. 2021.
PMID: 33917638
Free PMC article.
The Desmin (DES) Mutation p.A337P Is Associated with Left-Ventricular Non-Compaction Cardiomyopathy.
Kulikova O, Brodehl A, Kiseleva A, Myasnikov R, Meshkov A, Stanasiuk C, Gärtner A, Divashuk M, Sotnikova E, Koretskiy S, Kharlap M, Kozlova V, Mershina E, Pilus P, Sinitsyn V, Milting H, Boytsov S, Drapkina O.
Kulikova O, et al. Among authors: pilus p.
Genes (Basel). 2021 Jan 19;12(1):121. doi: 10.3390/genes12010121.
Genes (Basel). 2021.
PMID: 33478057
Free PMC article.
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[Familial left ventricular noncompaction: phenotypes and clinical course. Results of the multicenter registry].
Kulikova OV, Myasnikov RP, Mershina EA, Pilus PS, Koretskiy SN, Meshkov AN, Kiseleva AV, Kharlap MS, Sinitsyn VE, Sdvigova NA, Gandaeva LA, Barskiy VI, Derevnina YV, Zharova OP, Basargina EN, Boytsov SA, Drapkina OM.
Kulikova OV, et al. Among authors: pilus ps.
Ter Arkh. 2021 Apr 15;93(4):381-388. doi: 10.26442/00403660.2021.04.200677.
Ter Arkh. 2021.
PMID: 36286770
Russian.
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