Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Association of genetic variants in GABRA3 gene and thyrotoxic hypokalaemic periodic paralysis in Thai population.

Clinical endocrinology - 1 Apr 2008

Jongjaroenprasert Wallaya, Chanprasertyotin Suwannee, Butadej Siriwan, Nakasatien Soontaree, Charatcharoenwitthaya Natthinee, Himathongkam Thep, Ongphiphadhanakul Boonsong

Abstract excerpt

BACKGROUND: Genetic predisposition has been suggested to play role in the pathogenesis of thyrotoxic hypokalaemic periodic paralysis (THPP). OBJECTIVES: In this study, we assessed the differences of single-nucleotide polymorphisms (SNP) allelic frequency between THPP patients and well-characterized controls in order to find the susceptibility genetic variants related to THPP using microarray-based assessments on...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Genetic Predisposition to Disease
Share to Genetic Variation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Hyperthyroidism

Share to Hypokalemia

Share to Polymorphism, Single Nucleotide

Share to Receptors, GABA-A

Share to Thailand

Source

Identifiers

PMID: 17970773
DOI: 10.1111/j.1365-2265.2007.03083.x

Genes

GABRA3

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Association of genetic variants in GABRA3 gene and thyrotoxic hypokalaemic periodic paralysis in Thai population.PMID 17970773Read ↗

A genome-wide association study identifies novel susceptibility genetic variation for thyrotoxic hypokalemic periodic paralysis.Semantic proximity Read ↗

Genetic variant rs623011 (17q24.3) associates with non-familial thyrotoxic and sporadic hypokalemic paralysis.Semantic proximity Read ↗

Genome-wide meta-analysis reveals novel susceptibility loci for thyrotoxic periodic paralysis.Semantic proximity Read ↗

Genome-wide association study identifies a susceptibility locus for thyrotoxic periodic paralysis at 17q24.3.Semantic proximity Read ↗

Thyrotoxic periodic paralysis and polymorphisms of sodium-potassium ATPase genes.Semantic proximity Read ↗

Mutations in potassium channel Kir2.6 cause susceptibility to thyrotoxic hypokalemic periodic paralysis.Semantic proximity Read ↗

The clinical and genetic features in a cohort of mainland Chinese patients with thyrotoxic periodic paralysis.Semantic proximity Read ↗

A mutation in the KCNE3 potassium channel gene is associated with susceptibility to thyrotoxic hypokalemic periodic paralysis.Semantic proximity Read ↗

Genetic Screening of Patients with Thyrotoxic Hypokalemic Periodic Paralysis: An Experience from a Tertiary Care Hospital in the Northeast of Brazil.Semantic proximity Read ↗

Novel susceptibility gene for nonfamilial hypokalemic periodic paralysis.Semantic proximity Read ↗

Association of KCNJ2 Genetic Variants with Susceptibility to Thyrotoxic Periodic Paralysis in Patients with Graves' Disease.Semantic proximity Read ↗

Genetic analysis of 37 cases with primary periodic paralysis in Chinese patients.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.