Associated Papers
Genetics of BAG3: A Paradigm for Developing Precision Therapies for Dilated Cardiomyopathies.
Qu HQ et al.
Journal of the American Heart Association, 2022
36382946 (PubMed )
Supplement: JAH3-11-e027373-s001.pdf
Absence of Sac2/INPP5F enhances the phenotype of a Parkinson's disease mutation of synaptojanin 1.
Cao M et al.
Proceedings of the National Academy of Sciences of the United States of America, 2020
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