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Neonatal maternal separation delays the GABA excitatory-to-inhibitory functional switch by inhibiting KCC2 expression

While many of these mutations lead to the loss of transport function, the most common mutation, a deletion of phenylalanine (F) at residue 508 (F508), causes cystic fibrosis due to its rapid degradation at the ER (1)

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Kim, Dong-Hyun

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Not the seed, it was the sprouts