Mice with an NaV1.4 sodium channel null allele have latent myasthenia, without susceptibility to periodic paralysis.
about
Substitutions of the S4DIV R2 residue (R1451) in NaV1.4 lead to complex forms of paramyotonia congenita and periodic paralyses.Sodium Channelopathies of Skeletal Muscle.Dysfunction of NaV1.4, a skeletal muscle voltage-gated sodium channel, in sudden infant death syndrome: a case-control study.Hypokalaemic periodic paralysis and myotonia in a patient with homozygous mutation p.R1451L in NaV1.4.
P2860
Mice with an NaV1.4 sodium channel null allele have latent myasthenia, without susceptibility to periodic paralysis.
description
2016 nî lūn-bûn
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2016年の論文
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2016年論文
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2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
2016年论文
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2016年论文
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name
Mice with an NaV1.4 sodium cha ...... ibility to periodic paralysis.
@en
type
label
Mice with an NaV1.4 sodium cha ...... ibility to periodic paralysis.
@en
prefLabel
Mice with an NaV1.4 sodium cha ...... ibility to periodic paralysis.
@en
P2093
P2860
P356
P1433
P1476
Mice with an NaV1.4 sodium cha ...... ibility to periodic paralysis.
@en
P2093
P2860
P304
P356
10.1093/BRAIN/AWW070
P407
P50
P577
2016-04-05T00:00:00Z