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Autosomal Dominant Inherited Hearing Impairment Caused by a Missense Mutation in COL11A2 (DFNA13)

DOI

20

Citations

17

References

2001

Year

Els De Leenheer, Henricus P. M. Kunst, Wyman T. McGuirt, Sai Prasad, Matthew Brown, P.L.M. Huygen, Richard J. Smith, Cor W. R. J. Cremers
Archives of Otolaryngology - Head and Neck Surgery

Abstract

The trait in this family can be characterized as autosomal dominant, nonprogressive, presumably prelingual, midfrequency sensorineural hearing impairment.

References

YearCitations

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