
pmid: 27105111
Repeat expansions cause dominantly inherited neurological disorders. In this issue of Molecular Cell, Kearse et al. (2016) examine the requirements for RAN translation of the CGG repeats that cause fragile X-associated tremor/ataxia syndrome, revealing similarities and differences with canonical translation.
Fragile X Messenger Ribonucleoprotein 1, Fragile X Syndrome, Tremor, Humans, Ataxia
Fragile X Messenger Ribonucleoprotein 1, Fragile X Syndrome, Tremor, Humans, Ataxia
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