Concepedia

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Cochleovestibular and Ocular Features in a Dutch DFNA11 Family

DOI

21

Citations

10

References

2006

Year

Anne M.L.C. Bischoff, Ronald J. E. Pennings, P.L.M. Huygen, Mirjam W.J. Luijendijk, Erwin van Wijk, J.R.M. Cruysberg, Hannie Kremer, Cor W. R. J. Cremers
Otology & Neurotology

Abstract

Even though the diverse mutations are located in different regions of the myosin VIIa gene, the cochleovestibular phenotype is fairly similar in all DFNA11 families. Surprisingly, only in this family was subclinical retinal dysfunction detected.

References

YearCitations

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