Cite
HARVARD Citation
MacKenzie, K. et al. (2020). Goldberg–Shprintzen syndrome is determined by the absence, or reduced expression levels, of KIFBP. Human mutation. 41 (11), pp. 1906-1917. [Online].
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MacKenzie, K. et al. (2020). Goldberg–Shprintzen syndrome is determined by the absence, or reduced expression levels, of KIFBP. Human mutation. 41 (11), pp. 1906-1917. [Online].