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HARVARD Citation
Kuipers, D. et al. (2019). Late-onset phenotype associated with a homozygous GJC2 missense mutation in a Turkish family. Parkinsonism & related disorders. pp. 228-231. [Online].
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Kuipers, D. et al. (2019). Late-onset phenotype associated with a homozygous GJC2 missense mutation in a Turkish family. Parkinsonism & related disorders. pp. 228-231. [Online].