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Scnn1a
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Comprehensive mapping of Epithelial Na+ channel α expression in the mouse brain.
Presynaptic Homeostasis Opposes Disease Progression in Mouse Models of ALS-Like Degeneration: Eviden…
Novel homozygous mutation in SCNN1A gene in an Iranian boy with PHA1B.
Liddle Syndrome with a SCNN1A Mutation: A Case Report and Literature Review.
Pseudohypoaldosteronism Type 1b in a Saudi Female Infant Due to Homozygous Variant Gene Mutation in …
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Association of SCNN1A Single Nucleotide Polymorphisms With Neonatal Respiratory Distress Syndrome
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