Myotonia congenita mutation enhances the degradation of human CLC-1 chloride channels (Q28486132)

1

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Xiao-Dong Zhang

2

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Chao-Chin Chuang

3

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Jing-Jer Chen

4

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Yi-An Chen

5

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Shu-Ching Chen

6

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Tsung-Yu Chen

Creative Commons Attribution 4.0 International

7

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language of work or name

English

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publication date

2013

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published in

PLOS One

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volume

8

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page(s)

e55930

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issue

2

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copyright license

start time

12 February 2013

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

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describes a project that uses

ImageJ

1 reference

Europe PubMed Central

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC3570542/fullTextXML

inferred from PubMed Central ID database lookup

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Crossref

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0055930

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12 December 2020

Proteolysis: from the lysosome to ubiquitin and the proteasome

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12 December 2020

Disease-causing mutations C277R and C277Y modify gating of human ClC-1 chloride channels in myotonia congenita

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A distinct ER/IC gamma-secretase competes with the proteasome for cleavage of APP

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12 December 2020

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12 December 2020

Spectrum of CLCN1 mutations in patients with myotonia congenita in Northern Scandinavia

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12 December 2020

10.1371/JOURNAL.PONE.0055930

Identifiers

DOI

1 reference

3767150

ADS bibcode

2013PLoSO...855930L

0 references

3767150

1 reference

1 reference

1 reference