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HARVARD Citation
Jin, S. et al. (2019). SLC12A ion transporter mutations in sporadic and familial human congenital hydrocephalus*. Molecular genetics & genomic medicine. 7 (9), p. n/a. [Online].
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Jin, S. et al. (2019). SLC12A ion transporter mutations in sporadic and familial human congenital hydrocephalus*. Molecular genetics & genomic medicine. 7 (9), p. n/a. [Online].