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Article

Phenotypic Findings in Patients With KCNJ2-Related Anderson-Tawil Syndrome.

Neurology - 17 May 2022

O'Hare Meabh, Sadjadi Reza

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Potassium Channels, Inwardly Rectifying

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Identifiers

PMID: 35351792
DOI: 10.1212/WNL.0000000000200343

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

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Research trail→

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Phenotypic Findings in Patients With KCNJ2-Related Anderson-Tawil Syndrome.PMID 35351792Read ↗

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

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

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

Andersen-Tawil syndrome: a model of clinical variability, pleiotropy, and genetic heterogeneity.Semantic proximity Read ↗

Characterization of a novel KCNJ2 sequence variant detected in Andersen-Tawil syndrome patients.Semantic proximity Read ↗

Andersen-Tawil syndrome: prospective cohort analysis and expansion of the phenotype.Semantic proximity Read ↗

Phenotype variability in patients carrying KCNJ2 mutations.Semantic proximity Read ↗

Genotype-phenotype correlations of KCNJ2 mutations in Japanese patients with Andersen-Tawil syndrome.Semantic proximity Read ↗

Identification of the KCNJ2 Mutation in a Korean Family with Andersen-Tawil Syndrome and Developmental Delay.Semantic proximity Read ↗

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

Lack of any cardiac involvement in a patient with Andersen-Tawil syndrome associated with the c.574A→G mutation in KCNJ2.Semantic proximity Read ↗

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