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Erratum: Polymorphisms in KCNE1 or KCNE3 are not associated with Ménière disease in the Caucasian population

✍ Scribed by Colleen A. Campbell; Charley C. Della Santina; Nicole C. Meyer; Nancy B. Smith; Oluwaseun A. Myrie; Edwin M. Stone; Kuni Fukushima; Joseph Califano; John P. Carey; Marlan R. Hansen; Bruce J. Gantz; Lloyd B. Minor; Richard J.H. Smith

Publisher
John Wiley and Sons
Year
2011
Tongue
English
Weight
59 KB
Volume
155
Category
Article
ISSN
1552-4825

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Polymorphisms in KCNE1 or KCNE3 are not
Polymorphisms in KCNE1 or KCNE3 are not associated with Ménière disease in the Caucasian population
✍ Colleen A. Campbell; Charley C. Della Santina; Nicole C. Meyer; Nancy B. Smith; 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 English ⚖ 120 KB 👁 1 views

## Abstract Ménière disease (MD) is a complex disorder of unknown etiology characterized by the symptom triad of vertigo, sensorineural hearing loss, and tinnitus. Its reported incidence is 1–2 per 1,000 in Caucasians and 0.03–0.37 per 1,000 in Japanese. Doi et al. [Doi et al. (2005); ORL J Otorhin

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Maternal polymorphisms in folic acid metabolic genes are associated with nonsyndromic cleft lip and/or palate in the Brazilian population
✍ Andreia Bufalino; Lívia Máris Ribeiro Paranaíba; Sibele Nascimento de Aquino; He 📂 Article 📅 2010 🏛 John Wiley and Sons 🌐 English ⚖ 95 KB

BACKGROUND: Polymorphisms in genes that are involved in folic acid metabolism may be important maternal risk factors for the birth of a child with nonsyndromic cleft lip and/or palate (NSCL/P). The aim of this study was to determine the involvement of polymorphic variants in four genes (MTHFR, MTHFD