High prevalence of symptoms of Menière's disease in three families with a mutation in the COCH gene.

E Fransen; M Verstreken; W I Verhagen; F L Wuyts; P L Huygen; P D'Haese; N G Robertson; C C Morton; W T McGuirt; R J Smith

doi:10.1093/hmg/8.8.1425

High prevalence of symptoms of Menière's disease in three families with a mutation in the COCH gene.

NobleID: NI1P89W63R95S89
Persistent link: https://nobleid.org/ark:/48914/w1/20260515/CF852E2C

Type:Journal Article

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High prevalence of symptoms of Menière's disease in three families with a mutation in the COCH gene.

NobleID: NI1P89W63R95S89
Persistent link: https://nobleid.org/ark:/48914/w1/20260515/CF852E2C

Type:Journal Article

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