Harvard Catalyst Profiles

Contact, publication, and social network information about Harvard faculty and fellows.

Myo1c mutations associated with hearing loss cause defects in the interaction with nucleotide and actin.

Myo1c mutations associated with hearing loss cause defects in the interaction with nucleotide and actin. Cell Mol Life Sci. 2011 Jan; 68(1):139-50.

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Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.