rs80356697
|
|
|
0.710 |
GeneticVariation |
UNIPROT |
Mutations in dominant human myotonia congenita drastically alter the voltage dependence of the CIC-1 chloride channel.
|
8845168 |
1995 |
rs80356697
|
|
|
0.710 |
GeneticVariation |
UNIPROT |
ClC-1 mutations in myotonia congenita patients: insights into molecular gating mechanisms and genotype-phenotype correlation.
|
26096614 |
2015 |
rs80356697
|
|
|
0.710 |
GeneticVariation |
UNIPROT |
Novel muscle chloride channel (CLCN1) mutations in myotonia congenita with various modes of inheritance including incomplete dominance and penetrance.
|
9566422 |
1998 |
rs80356697
|
|
|
0.710 |
GeneticVariation |
UNIPROT |
Decrement of compound muscle action potential is related to mutation type in myotonia congenita.
|
12661046 |
2003 |
rs80356697
|
|
|
0.710 |
GeneticVariation |
UNIPROT |
A case of non-dystrophic myotonia with concomitant mutations in the SCN4A and CLCN1 genes.
|
27653901 |
2016 |
rs80356697
|
|
|
0.710 |
GeneticVariation |
UNIPROT |
Thomsen disease with ptosis and abnormal MR findings.
|
27666773 |
2016 |
rs80356697
|
|
|
0.710 |
GeneticVariation |
UNIPROT |
Molecular basis of Thomsen's disease (autosomal dominant myotonia congenita).
|
7981750 |
1993 |
rs80356697
|
|
|
0.710 |
GeneticVariation |
UNIPROT |
Myotonia levior is a chloride channel disorder.
|
7581380 |
1995 |
rs80356697
|
|
|
0.710 |
GeneticVariation |
UNIPROT |
Spectrum of mutations in the major human skeletal muscle chloride channel gene (CLCN1) leading to myotonia.
|
8533761 |
1995 |
rs80356697
|
|
|
0.710 |
GeneticVariation |
UNIPROT |
ClC-1 chloride channel mutations in myotonia congenita: variable penetrance of mutations shifting the voltage dependence.
|
9736777 |
1998 |
rs80356697
|
|
|
0.710 |
GeneticVariation |
UNIPROT |
A mutation in autosomal dominant myotonia congenita affects pore properties of the muscle chloride channel.
|
9122265 |
1997 |
rs80356697
|
|
|
0.710 |
GeneticVariation |
UNIPROT |
Multimeric structure of ClC-1 chloride channel revealed by mutations in dominant myotonia congenita (Thomsen).
|
8112288 |
1994 |
rs80356697
|
|
|
0.710 |
GeneticVariation |
BEFREE |
A parallel was drawn between this unprecedented situation and that of myotonia congenita by including patients homozygous or heterozygous for the CLCN1 I556N channel mutation, which is known for incomplete dominance and penetrance.
|
19882638 |
2010 |