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APA Citation
Khodadadi, H., Azcona, L. J., Aghamollaii, V., Omrani, M. D., Garshasbi, M., Taghavi, S., Tafakhori, A., Shahidi, G. A., Jamshidi, J., Darvish, H., & Paisán‐Ruiz, C. (2017). pTRHD1 (C2orf79) mutations lead to autosomal‐recessive intellectual disability and parkinsonism. Movement disorders, 32(2), 287–291. http://access.bl.uk/ark:/81055/vdc_100041943011.0x000034