英语词汇“myotonia”的意思、用法、释义、翻译、读音、例句、短语、词组-英语词典

是什么意思

肌强直；

英英释义

myotonia[ ,mai?u't?uni? ]

n.abnormally long muscular contractions; slow relaxation of a muscle after a contraction

学习怎么用

权威例句

Myotonia caused by mutations in the muscle chloride channel gene CLCN1
Membrane changes in cells from myotonia patients.
Molecular basis of Thomsen's disease (autosomal dominant myotonia congenita)
Human sodium channel myotonia: slowed channel inactivation due to substitutions for a glycine within the III-IV linker
The skeletal muscle chloride channel in dominant and recessive human myotonia
Adynamia episodica hereditaria with myotonia: A non-inactivating sodium current and the effect of extracellular pH
Reversal of RNA Missplicing and Myotonia after Muscleblind Overexpression in a Mouse Poly(CUG) Model for Myotonic Dystrophy
Correction of ClC-1 splicing eliminates chloride channelopathy and myotonia in mouse models of myotonic dystrophy.
Sodium channel mutations in acetazolamide‐responsive myotonia congenita, paramyotonia congenita, and hyperkalemic periodic paralysis
Multimeric structure of ClC-1 chloride channel revealed by mutations in dominant myotonia congenita (Thomsen)

单词	myotonia
释义	myotonia 听听怎么读英 [?ma??'t??n??] 美 [?ma??'to?n?r] 是什么意思 n. 肌强直；英英释义 myotonia[ ,mai?u't?uni? ] n.abnormally long muscular contractions; slow relaxation of a muscle after a contraction 学习怎么用权威例句 Myotonia caused by mutations in the muscle chloride channel gene CLCN1 Membrane changes in cells from myotonia patients. Molecular basis of Thomsen's disease (autosomal dominant myotonia congenita) Human sodium channel myotonia: slowed channel inactivation due to substitutions for a glycine within the III-IV linker The skeletal muscle chloride channel in dominant and recessive human myotonia Adynamia episodica hereditaria with myotonia: A non-inactivating sodium current and the effect of extracellular pH Reversal of RNA Missplicing and Myotonia after Muscleblind Overexpression in a Mouse Poly(CUG) Model for Myotonic Dystrophy Correction of ClC-1 splicing eliminates chloride channelopathy and myotonia in mouse models of myotonic dystrophy. Sodium channel mutations in acetazolamide‐responsive myotonia congenita, paramyotonia congenita, and hyperkalemic periodic paralysis Multimeric structure of ClC-1 chloride channel revealed by mutations in dominant myotonia congenita (Thomsen)
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