Cite
HARVARD Citation
Stödberg, T. et al. (2020). SLC12A2 mutations cause NKCC1 deficiency with encephalopathy and impaired secretory epithelia. Neurology. p. . [Online].
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Stödberg, T. et al. (2020). SLC12A2 mutations cause NKCC1 deficiency with encephalopathy and impaired secretory epithelia. Neurology. p. . [Online].