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Case report: A Chinese child with Andersen-Tawil syndrome due to a de novo KCNJ2 mutation.

Journal of the neurological sciences - 15 May 2015

Liu Xiao-Li, Huang Xiao-Jun, Luan Xing-Hua, Zhou Hai-Yan, Wang Tian, Wang Jing-Yi, Shen Jun-Yi, Chen Sheng-di, Tang Hui-Dong, Cao Li

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 25847018
DOI: 10.1016/j.jns.2015.02.027

Genes

KCNJ2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 3 Sept 2026.

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Case report: A Chinese child with Andersen-Tawil syndrome due to a de novo KCNJ2 mutation.PMID 25847018Read ↗

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Mutations of KCNJ2 gene associated with Andersen-Tawil syndrome in Korean families.Semantic proximity Read ↗

Phenotypic Variability of Andersen-Tawil Syndrome Due to Allelic Mutation c.652C>T in the KCNJ2 Gene-A New Family Case Report.Semantic proximity Read ↗

A novel neuropsychiatric phenotype of KCNJ2 mutation in one Taiwanese family with Andersen-Tawil syndrome.Semantic proximity Read ↗

Compound heterozygous mutations in KCNJ2 and KCNH2 in a patient with severe Andersen-Tawil syndrome.Semantic proximity Read ↗

KID syndrome in a Malaysian child with identification of novel heterozygous missense mutation GJB2 c.581T>A(p. 194Phe>Tyr).Semantic proximity Read ↗

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A new homozygous mutation of the KCNQ1 gene associated with both Romano-Ward and incomplete Jervell Lange-Nielsen syndromes in two sisters.Semantic proximity Read ↗

Andersen-Tawil syndrome: clinical and molecular aspects.Semantic proximity Read ↗

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