A common founder for the 35delG GJB2gene mutation in connexin 26 hearing impairment | Journal of Medical Genetics

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A common founder for the 35delG GJB2gene mutation in connexin 26 hearing impairment

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Cite this article as:: Van Laer L, Coucke P, Mueller RF, et al

A common founder for the 35delG GJB2gene mutation in connexin 26 hearing impairment

Journal of Medical Genetics 2001;38:515-518.