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HARVARD Citation
Shalash, A. et al. (2017). C.207C>G mutation in sepiapterin reductase causes autosomal dominant dopa-responsive dystonia. Neurology. p. . [Online].
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Shalash, A. et al. (2017). C.207C>G mutation in sepiapterin reductase causes autosomal dominant dopa-responsive dystonia. Neurology. p. . [Online].