Cite
HARVARD Citation
Khodadadi, H. et al. (2017). PTRHD1 (C2orf79) mutations lead to autosomal‐recessive intellectual disability and parkinsonism. Movement disorders. 32 (2), pp. 287-291. [Online].
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Khodadadi, H. et al. (2017). PTRHD1 (C2orf79) mutations lead to autosomal‐recessive intellectual disability and parkinsonism. Movement disorders. 32 (2), pp. 287-291. [Online].