The phenotype of DFNA13/: Nonsyndromic autosomal dominant mid-frequency and high-frequency sensorineural hearing impairment

descriptionPublicationkeyboard_double_arrow_right Article 01 Mar 2000 English Publisher:Elsevier BVJournal:American Journal of Otolaryngology, volume 21, pages 181-187 (issn: 0196-0709,

Authors: H KUNST; C HUYBRECHTS; H MARRES; P HUYGEN; G VANCAMP; C CREMERS;

doi: 10.1016/s0196-0709(00)80006-x

The phenotype of DFNA13/: Nonsyndromic autosomal dominant mid-frequency and high-frequency sensorineural hearing impairment

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The phenotype of DFNA13/: Nonsyndromic autosomal dominant mid-frequency and high-frequency sensorineural hearing impairment

The phenotype of DFNA13/: Nonsyndromic autosomal dominant mid-frequency and high-frequency sensorineural hearing impairment

4 Research products, page 1 of 1

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

The phenotype of DFNA13/COL11A2: nonsyndromic autosomal dominant mid-frequency and high-frequency sensorineural hearing impairment.

A Dutch family with progressive autosomal dominant non-syndromic sensorineural hearing impairment linked to DFNA13

Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13)