๐ค Sergey Y Kleymenov
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The D75N and P161S Mutations in the C0-C2 Fragment of cMyBP-C Associated with Hypertrophic Cardiomyopathy Disturb the Thin Filament Activation, Nucleotide Exchange in Myosin, and Actin-Myosin Interaction.
๐ค
Anastasia M Kochurova
,
Evgenia A Beldiia
,
Victoria V Nefedova
+10 more
ยท 2024 ยท International journal of molecular sciences ยท MDPI
ยท added 2026-04-24
Anastasia M Kochurova
,
Evgenia A Beldiia
,
Victoria V Nefedova
,
Daria S Yampolskaya
,
Natalia A Koubassova
,
Sergey Y Kleymenov
,
Julia Y Antonets
,
Natalia S Ryabkova
,
Ivan A Katrukha
,
Sergey Y Bershitsky
,
Alexander M Matyushenko
,
Galina V Kopylova
,
Daniil V Shchepkin
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About half of the mutations that lead to hypertrophic cardiomyopathy (HCM) occur in the
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DOI:
10.3390/ijms252011195
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MYBPC3
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