Functional variants in NOS1 and NOS2A are not associated with progressive hearing loss in Ménière's disease in a European Caucasian population.
Gazquez I, Lopez-Escamez JA, Moreno A, Campbell CA, Meyer NC, Carey JP, Minor LB, Gantz BJ, Hansen MR, Della Santina CC, Aran I, Soto-Varela A, Santos S, Batuecas A, Perez-Garrigues H, Lopez-Nevot A, Smith RJ, Lopez-Nevot MA.
Gazquez I, et al.
DNA Cell Biol. 2011 Sep;30(9):699-708. doi: 10.1089/dna.2011.1259. Epub 2011 May 25.
DNA Cell Biol. 2011.
PMID: 21612410
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