Progressive hearing loss, and recurrent sudden sensorineural hearing loss associated with GJB2 mutations – phenotypic spectrum and frequencies of GJB2 mutations in Austria

No abstract is available for this paper.

• Publication year

  2002

• Venue

  Human Genetics

• Publication date

  2002-07-03

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1007/s00439-002-0762-yPMID 12189487
• 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.

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