Harvard Catalyst Profiles

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

A tRNA(Ala) mutation causing mitochondrial myopathy clinically resembling myotonic dystrophy.

A tRNA(Ala) mutation causing mitochondrial myopathy clinically resembling myotonic dystrophy. J Med Genet. 2003 Oct; 40(10):752-7.

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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.