Functional variants of MIF, INFG and TFNA genes are not associated with disease susceptibility or hearing loss progression in patients with Ménière’s disease-Reference-Cited by-同舟云学术

Functional variants of MIF, INFG and TFNA genes are not associated with disease susceptibility or hearing loss progression in patients with Ménière’s disease

Published:2012-11-21 Issue:4 Volume:270 Page:1521-1529
ISSN:0937-4477
Container-title:European Archives of Oto-Rhino-Laryngology
language:en
Short-container-title:Eur Arch Otorhinolaryngol

Author:

Gázquez Irene,Moreno Antonia,Requena Teresa,Ohmen Jeff,Santos-Perez Sofia,Aran Ismael,Soto-Varela Andres,Pérez-Garrigues Herminio,López-Nevot Alicia,Batuecas Angel,Friedman Rick A.,López-Nevot Miguel A.,López-Escamez Jose A.

Publisher

Springer Science and Business Media LLC

Subject

General Medicine,Otorhinolaryngology

Link

http://link.springer.com/content/pdf/10.1007/s00405-012-2268-0.pdf

Reference41 articles.

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3. Avan P, Giraudet F, Chauveau B, Gilain L, Mom T (2011) Unstable distortion-product otoacoustic emission phase in Menière’s disease. Hear Res 277:88–95

4. Baugh JA, Chitnis S, Donnelly SC, Monteiro J, Lin X, Plant BJ, Wolfe F, Gregersen PK, Bucala R (2002) A functional promoter polymorphism in the macrophage migration inhibitory factor (MIF) gene associated with disease severity in rheumatoid arthritis. Genes Immun 3:170–176

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