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pro vyhledávání: '"Andrew Scott Terker"'
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 10 (2022)
Loss-of-function mutations in the human potassium chloride cotransporter-3 (KCC3) cause a hereditary motor sensory neuropathy associated with agenesis of the corpus callosum. While recapitulating the neuropathy, KCC3-knockout mice also exhibit high b
Externí odkaz:
https://doaj.org/article/99fed9096d724cdb9184daf0a396615a
