Polymorphisms in KCNE1 or KCNE3 are not associated with Ménière disease in the Caucasian population
about
Deep resequencing of the voltage-gated potassium channel subunit KCNE3 gene in chronic tinnitusGenetics of vestibular disorders: pathophysiological insightsIon homeostasis in the ear: mechanisms, maladies, and management.Cellular and molecular mechanisms of autosomal dominant form of progressive hearing loss, DFNA2.Intronic variants in the NFKB1 gene may influence hearing forecast in patients with unilateral sensorineural hearing loss in Meniere's diseaseThe genetics of Ménière's disease.Genetic disorders of the vestibular system.Genetics of recurrent vertigo and vestibular disordersPolymorphisms in genes involved in oxidative stress response in patients with sudden sensorineural hearing loss and Ménière's disease in a Japanese population.KCNE1 and KCNE3: The yin and yang of voltage-gated K(+) channel regulationAn Examination of KCNE1 Mutations and Common Variants in Chronic Tinnitus.A replication study on proposed candidate genes in Ménière's disease, and a review of the current status of genetic studies.Variants in the KCNE1 or KCNE3 gene and risk of Ménière's disease: A meta-analysis.The aetiopathologies of Ménière's disease: a contemporary review.Genetics of ion homeostasis in Ménière's Disease.Polymorphisms in genes involved in the free-radical process in patients with sudden sensorineural hearing loss and Ménière's disease.Association between polymorphisms in genes encoding methylenetetrahydrofolate reductase and the risk of Ménière's disease.Association of interleukin-1 gene polymorphisms with sudden sensorineural hearing loss and Ménière's disease.
P2860
Q21203797-68EF38E5-39BE-4542-8116-43B178640147Q26753131-0C142207-7641-4BAE-904D-AD70F8848D49Q30473907-DD1F9593-ED6B-493A-8717-4D0350E8FB84Q30497891-6FDE5AF3-2ECB-474B-97F3-9713308267A9Q34513628-F92BF98B-0F47-4DB6-A2F6-D59B46BA28DDQ34952111-BFA350C6-0A0D-40F0-B10D-7F017308C643Q35133047-FC984AFB-AE2B-4C0B-9B01-46A392E3FF27Q35228799-75E0CBAD-30D8-43F4-96CD-C5F50273A253Q36280856-A14E4883-08AE-474E-9EAE-79B4BF6CC99AQ37028794-CB1E3221-0984-4503-9151-B6E68661834FQ37651406-BE73829E-A807-4058-9B92-B8E39EA903F8Q38039210-D5426838-AFCB-48A7-B7B4-FA1F00988AE7Q38738939-E6A8D19A-53E3-430C-879E-CF2B1688E098Q39154221-B2854718-B328-458E-860A-BB247654F7CBQ39193364-F7034087-894A-413D-876D-C45C3BD06DD7Q50357355-14233884-6790-4901-954D-DCA1C4B70E91Q50357471-EE5639EE-DF83-424B-9B7D-89D0C206CADFQ50434669-26274226-7815-49A4-8DDF-A3756BE78A95
P2860
Polymorphisms in KCNE1 or KCNE3 are not associated with Ménière disease in the Caucasian population
description
2010 nî lūn-bûn
@nan
2010 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Polymorphisms in KCNE1 or KCNE ...... se in the Caucasian population
@ast
Polymorphisms in KCNE1 or KCNE ...... se in the Caucasian population
@en
Polymorphisms in KCNE1 or KCNE ...... se in the Caucasian population
@nl
type
label
Polymorphisms in KCNE1 or KCNE ...... se in the Caucasian population
@ast
Polymorphisms in KCNE1 or KCNE ...... se in the Caucasian population
@en
Polymorphisms in KCNE1 or KCNE ...... se in the Caucasian population
@nl
prefLabel
Polymorphisms in KCNE1 or KCNE ...... se in the Caucasian population
@ast
Polymorphisms in KCNE1 or KCNE ...... se in the Caucasian population
@en
Polymorphisms in KCNE1 or KCNE ...... se in the Caucasian population
@nl
P2093
P2860
P50
P3181
P356
P1476
Polymorphisms in KCNE1 or KCNE ...... se in the Caucasian population
@en
P2093
Charley C Della Santina
John P Carey
Joseph Califano
Kuni Fukushima
Lloyd B Minor
Nancy B Smith
Nicole C Meyer
Oluwaseun A Myrie
Richard J H Smith
P2860
P3181
P356
10.1002/AJMG.A.33114
P407
P577
2010-01-01T00:00:00Z