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Szczałuba, K. et al. (2018). A de novo loss‐of‐function DYNC1H1 mutation in a patient with parkinsonian features and a favourable response to levodopa. Clinical genetics. 93 (5), pp. 1107-1108. [Online].
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Szczałuba, K. et al. (2018). A de novo loss‐of‐function DYNC1H1 mutation in a patient with parkinsonian features and a favourable response to levodopa. Clinical genetics. 93 (5), pp. 1107-1108. [Online].