ArticleBMC medical genetics2015
An atypical form of AOA2 with myoclonus associated with mutations in SETX and AFG3L2.
Cecilia Mancini et al.PubMed ↗Full text ↗Publisher ↗
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ArticleBMC medical genetics2015
Cecilia Mancini et al.PubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.