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APA Citation
Petry-Schmelzer, J., Keller, N., Karakaya, M., Wirth, B., Fink, G., & Wunderlich, G. (2021). p 27. VPS13D: One family, one mutation, two phenotypes. Clinical neurophysiology, 132(8), e12–e13. http://access.bl.uk/ark:/81055/vdc_100134864333.0x00001a