The phenotype of DFNA13/COL11A2.

No abstract is available for this paper.

• Publication year

  2001

• Venue

  Advances in Oto-Rhino-Laryngology

• Publication date

  2001-08-01

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1046/J.1365-2273.2001.00479-16.XPMID 12408068
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

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

  1999cited by this paper

• Nonsyndromic Hearing Loss Caused by USH1G Mutations: Widening the USH1G Disease Spectrum

  2015cites this paper
• Similar Phenotypes Caused by Mutations in OTOG and OTOGL

  2014cites this paper
• Hearing impairment in Stickler syndrome: a systematic review

  2012cites this paper
• Mutations of the gene encoding otogelin are a cause of autosomal-recessive nonsyndromic moderate hearing impairment.

  2012cites this paper
• Audioprofiling identifies TECTA and GJB2‐related deafness segregating in a single extended pedigree

  2007influential citation
• Mutation analysis of COL9A3, a gene highly expressed in the cochlea, in hearing loss patients.

  2005cites this paper
• Genética molecular da deficiência auditiva não-sindrômica

  2005cites this paper
• Molecular genetics of non-syndromic deafness

  2005cites this paper
• Molecular genetics of non-syndromic deafness Summary

  2005cites this paper
• Audiological Characteristics of Some Affected Members of a Dutch DFNA13/COL11A2 Family

  2004cites this paper
• Minor cartilage collagens : characterization of the human COL9A1, COL9A2 and COL11A2 genes and the mouse Col11a2 gene. Identification of a mutation in the COL11A2 gene in a family with non-ocular Stickler syndrome

  2003cites this paper
• Nonsyndromic Hearing Loss

  2003cites this paper