| scholarly article | Q13442814 |
| P356 | DOI | 10.1038/JHG.2012.20 |
| P698 | PubMed publication ID | 22399142 |
| P50 | author | Yūsuke Nakamura | Q11365872 |
| Naoyuki Kamatani | Q29839679 | ||
| Surakameth Mahasirimongkol | Q41653574 | ||
| Michiaki Kubo | Q42316443 | ||
| P2093 | author name string | Atsushi Takahashi | |
| Boonsong Ongphiphadhanakul | |||
| Taisei Mushiroda | |||
| Nattiya Hirankarn | |||
| Suwannee Chanprasertyotin | |||
| Thiti Snabboon | |||
| Wallaya Jongjaroenprasert | |||
| Supamai Soonthornpun | |||
| Thep Himathongkam | |||
| Puntip Tantiwong | |||
| Paninee Rattanapichart | |||
| Sunee Mamanasiri | |||
| Theerawut Phusantisampan | |||
| P2860 | cites work | Population structure and eigenanalysis | Q21145248 |
| Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen's syndrome | Q24291252 | ||
| Mutations in potassium channel Kir2.6 cause susceptibility to thyrotoxic hypokalemic periodic paralysis | Q24295040 | ||
| The International HapMap Project | Q27860695 | ||
| Haploview: analysis and visualization of LD and haplotype maps | Q27860955 | ||
| MiRP2 forms potassium channels in skeletal muscle with Kv3.4 and is associated with periodic paralysis | Q28201439 | ||
| Genetic and functional linkage of Kir5.1 and Kir2.1 channel subunits | Q28203905 | ||
| Genevar: a database and Java application for the analysis and visualization of SNP-gene associations in eQTL studies | Q33654995 | ||
| SNPexp - A web tool for calculating and visualizing correlation between HapMap genotypes and gene expression levels | Q33774611 | ||
| Voltage-sensor sodium channel mutations cause hypokalemic periodic paralysis type 2 by enhanced inactivation and reduced current | Q35208537 | ||
| Long range chromatin interactions involved in gene regulation | Q37245023 | ||
| No mutation in the KCNE3 potassium channel gene in Chinese thyrotoxic hypokalaemic periodic paralysis patients. | Q47305399 | ||
| Association of novel single nucleotide polymorphisms in the calcium channel alpha 1 subunit gene (Ca(v)1.1) and thyrotoxic periodic paralysis | Q47998641 | ||
| A novel sodium channel mutation in a family with hypokalemic periodic paralysis | Q55670198 | ||
| HLA and thyrotoxic periodic paralysis. | Q55690442 | ||
| A high-throughput SNP typing system for genome-wide association studies | Q57269468 | ||
| Arg16Gly polymorphism in beta2-adrenergic receptor gene is not associated with thyrotoxic periodic paralysis in Korean male patients with Graves' disease | Q57762278 | ||
| Clinical and Molecular Analysis of Chinese Patients with Thyrotoxic Periodic Paralysis | Q64460776 | ||
| Mapping of the hypokalaemic periodic paralysis (HypoPP) locus to chromosome 1q31-32 in three European families | Q72017458 | ||
| Prospects for whole-genome linkage disequilibrium mapping of common disease genes | Q77883184 | ||
| Mutation screening in Chinese hypokalemic periodic paralysis patients | Q82140254 | ||
| P4510 | describes a project that uses | genome-wide association study | Q1098876 |
| P433 | issue | 5 | |
| P921 | main subject | genetic variation | Q349856 |
| hypokalemic periodic paralysis | Q622828 | ||
| genome-wide association study | Q1098876 | ||
| P304 | page(s) | 301-304 | |
| P577 | publication date | 2012-03-08 | |
| P1433 | published in | Journal of Human Genetics | Q6295302 |
| P1476 | title | A genome-wide association study identifies novel susceptibility genetic variation for thyrotoxic hypokalemic periodic paralysis | |
| P478 | volume | 57 |
| Q37212986 | A 10-year analysis of thyrotoxic periodic paralysis in 135 patients: focus on symptomatology and precipitants |
| Q64241967 | Assessment of Molecular Subtypes in Thyrotoxic Periodic Paralysis and Graves Disease Among Chinese Han Adults: A Population-Based Genome-Wide Association Study |
| Q34041126 | Copy number variation in Thai population |
| Q84730497 | Genome-wide association study identifies a susceptibility locus for thyrotoxic periodic paralysis at 17q24.3. |
| Q99582580 | Impact of first-line treatment choice on long-term outcomes of hyperthyroid Graves' disease patients with thyrotoxic periodic paralysis |
| Q34872431 | Insight in genome-wide association of metabolite quantitative traits by exome sequence analyses |
| Q38217762 | Inward-rectifying potassium channelopathies: new insights into disorders of sodium and potassium homeostasis |
| Q51751840 | Novel lincRNA Susceptibility Gene and Its Role in Etiopathogenesis of Thyrotoxic Periodic Paralysis. |
| Q50470772 | Severe exacerbation of Andersen-Tawil syndrome secondary to thyrotoxicosis. |
| Q35212193 | The clinical and genetic features in a cohort of mainland Chinese patients with thyrotoxic periodic paralysis |
| Q26744730 | Therapeutic Approaches to Genetic Ion Channelopathies and Perspectives in Drug Discovery |
| Q38037461 | Thyrotoxic periodic paralysis: clinical and molecular aspects |
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