The Startle Disease Mutation E103K Impairs Activation of Human Homomeric α1 Glycine Receptors by Disrupting an Intersubunit Salt Bridge across the Agonist Binding Site.
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The Startle Disease Mutation E103K Impairs Activation of Human Homomeric α1 Glycine Receptors by Disrupting an Intersubunit Salt Bridge across the Agonist Binding Site.
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2017 nî lūn-bûn
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2017年の論文
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name
The Startle Disease Mutation E ...... ross the Agonist Binding Site.
@en
The Startle Disease Mutation E ...... ross the Agonist Binding Site.
@nl
type
label
The Startle Disease Mutation E ...... ross the Agonist Binding Site.
@en
The Startle Disease Mutation E ...... ross the Agonist Binding Site.
@nl
prefLabel
The Startle Disease Mutation E ...... ross the Agonist Binding Site.
@en
The Startle Disease Mutation E ...... ross the Agonist Binding Site.
@nl
P2093
P2860
P50
P356
P1476
The Startle Disease Mutation E ...... ross the Agonist Binding Site.
@en
P2093
David Jane
Elliot Hurdiss
Fatemah Safar
Guangyu Fang
Marios Erotocritou
P2860
P304
P356
10.1074/JBC.M116.767616
P407
P577
2017-02-07T00:00:00Z