Pathological and genetic analysis of the degenerating muscle (dmu) mouse: a new allele of Scn8a
Author:
Publisher
Oxford University Press (OUP)
Subject
Genetics (clinical),Genetics,Molecular Biology,General Medicine
Link
http://academic.oup.com/hmg/article-pdf/10/17/1819/9813519/101819.pdf
Cited by 18 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Association of respiratory failure with inhibition of NaV1.6 in the phrenic nerve;Channels;2022-10-14
2. Mice Heterozygous for the Sodium Channel Scn8a (Nav1.6) Have Reduced Inflammatory Responses During EAE and Following LPS Challenge;Frontiers in Immunology;2021-03-19
3. Voltage‐gated sodium channel‐dependent retroaxonal modulation of photoreceptor function during post‐natal development in mice;Developmental Neurobiology;2021-02-23
4. Mutations in theScn8aDIIS4 voltage sensor reveal new distinctions among hypomorphic and null Nav1.6 sodium channels;Genes, Brain and Behavior;2020-04
5. Mutations of Sodium Channel SCN8A (Nav1.6) in Neurological Disease;Ion Channels in Health and Disease;2016
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