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Article Review/Hyperlink
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Estivill X, Fortina P, Surrey S, Rabionet R, Melchionda S, et
al
Connexin-26 mutations in sporadic and inherited
sensorineural deafness
Lancet
(Feb) 351:394-398 1998

Nothing to do with nephrology directly in this paper, but the new findings
regarding the genetic
origins of non-syndromic deafness may be of interest to nephrologists
considering a possible
diagnosis of hereditary deafness-kidney disease syndromes.
The abstract of this paper is available from the National Library of
Medicine's PubMed site:
click here .
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