Associated Papers
A novel missense mutation in the ACTG1 gene in a family with congenital autosomal dominant deafness: A case report.
Lee CG et al.
Molecular Medicine Reports, 2018
The Relay/Converter Interface Influences Hydrolysis of ATP by Skeletal Muscle Myosin II.
Bloemink MJ et al.
The Journal of Biological Chemistry, 2016
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