The Phe932Ile mutation in KCNT1 channels associated with severe epilepsy, delayed myelination and leukoencephalopathy produces a loss-of-function channel phenotype.
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The Phe932Ile mutation in KCNT1 channels associated with severe epilepsy, delayed myelination and leukoencephalopathy produces a loss-of-function channel phenotype.
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name
The Phe932Ile mutation in KCNT ...... of-function channel phenotype.
@en
The Phe932Ile mutation in KCNT ...... of-function channel phenotype.
@nl
type
label
The Phe932Ile mutation in KCNT ...... of-function channel phenotype.
@en
The Phe932Ile mutation in KCNT ...... of-function channel phenotype.
@nl
prefLabel
The Phe932Ile mutation in KCNT ...... of-function channel phenotype.
@en
The Phe932Ile mutation in KCNT ...... of-function channel phenotype.
@nl
P2860
P1433
P1476
The Phe932Ile mutation in KCNT ...... of-function channel phenotype.
@en
P2093
Arin Bhattacharjee
Katherine M Evely
P2860
P356
10.1016/J.NEUROSCIENCE.2017.03.035
P407
P577
2017-03-31T00:00:00Z