Identified seven mutations in the MyoVA motor domain responsible for viable dilute alleles in mice, providing insights into motor domain function.
No takes yet. Share an insight, caveat, or question.
Offers viable mouse models for MyoVA motor domain analysis; leaves open human disease translation.
Huang et al. (1998) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: