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espn protein, human
(compound)
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Autosomal dominant Alport syndrome due to a COL4A4 mutation with an additional ESPN variant detected…
Integrative analysis of DNA methylation and gene expression profiles identified potential breast can…
Characterization and regulation of an additional actin-filament-binding site in large isoforms of th…
Targeting of the hair cell proteins cadherin 23, harmonin, myosin XVa, espin, and prestin in an epit…
A novel mutation in the Espin gene causes autosomal recessive nonsyndromic hearing loss but no appar…
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