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P.M. Kelley

Center for the Study of Hereditary Hearing Loss

Boys Town National Research Hospital

Omaha

USA

[email]@boystown.org

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Affiliation

Center for the Study of Hereditary Hearing Loss, Boys Town National Research Hospital, Omaha, USA. 1998 - 1999

References

Human connexin 30 (GJB6), a candidate gene for nonsyndromic hearing loss: molecular cloning, tissue-specific expression, and assignment to chromosome 13q12. Kelley, P.M., Abe, S., Askew, J.W., Smith, S.D., Usami, S., Kimberling, W.J. Genomics (1999) [Pubmed]
Novel mutations in the connexin 26 gene (GJB2) that cause autosomal recessive (DFNB1) hearing loss. Kelley, P.M., Harris, D.J., Comer, B.C., Askew, J.W., Fowler, T., Smith, S.D., Kimberling, W.J. Am. J. Hum. Genet. (1998) [Pubmed]