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spectrins
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Mouse Phenotypes - Hereditary spherocytosis
OMIM - Congenital disorder
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Spectrins: molecular organizers and targets of neurological disorders.
Heterozygous Missense Pathogenic Variants Within the Second Spectrin Repeat of SPTBN2 Lead to Infant…
Complementary mesoscale dynamics of spectrin and acto-myosin shape membrane territories during mecha…
Nuclear mechanical resilience but not stiffness is modulated by αII-spectrin.
Outer hair cell function is normal in βV spectrin knockout mice.
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A Novel Mutation of the Spectrin Gene
Safety, Tolerability and the Effects on Cerebrospinal Fluid Spectrin Breakdown Product-145 Levels of…
Hemolysis in Patients With Hereditary Spherocytosis (HS)
Safety and Antiviral Activity of BLD-2660 in COVID-19 Hospitalized Subjects
Biomarker Levels as A Predictor of Concussion Severity OUTcomes (BlacOut)
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