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Updated: Mar 1, 2026

07:59
Functional Characterization of Endogenously Expressed Human RYR1 Variants
Published on: June 9, 2021
3.1K
A novel homozygous splice-site mutation in RYR1 causes fetal hydrops and affects skeletal and smooth muscle
Nicole Meier1,2,3, Elisabeth Bruder3,4, Isabel Filges1,2,3
1Medical Genetics, University Hospital Basel, Basel, Switzerland.
Prenatal Diagnosis
|May 26, 2017
Abstract
No abstract available in PubMed .
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