Stödberg, T., Magnusson, M., Lesko, N., Wredenberg, A., Martin Munoz, D., Stranneheim, H., & Wedell, A. (2020). SLC12A2 mutations cause NKCC1 deficiency with encephalopathy and impaired secretory epithelia. Neurol Genet.

Stödberg, Tommy, Måns Magnusson, Nicole Lesko, Anna Wredenberg, Daniel Martin Munoz, Henrik Stranneheim, and Anna Wedell. "SLC12A2 Mutations Cause NKCC1 Deficiency With Encephalopathy and Impaired Secretory Epithelia." Neurol Genet 2020.

Stödberg, Tommy, et al. "SLC12A2 Mutations Cause NKCC1 Deficiency With Encephalopathy and Impaired Secretory Epithelia." Neurol Genet 2020.