(Q24601791)

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Channelopathies

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Europe PubMed Central

Channelopathies (English)

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June-Bum Kim

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January 2014

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Korean journal of pediatrics

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57

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1-18

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Creative Commons Attribution-NonCommercial 3.0 Unported

1 January 2014

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April 2022 Public Data File from Crossref

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https://pubmed.ncbi.nlm.nih.gov/24578711

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based on heuristic

inferred from PubMed ID database lookup

Reduced expression of Kir6.2/SUR2A subunits explains KATP deficiency in K+-depleted rats

1 reference

https://pubmed.ncbi.nlm.nih.gov/24578711

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.3345/KJP.2014.57.1.1

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PMC publication ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PubMed publication ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

ResearchGate publication ID

0 references

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