Free Access
| Issue |
Med Sci (Paris)
Volume 18, Number 8-9, Août–Septembre 2002
|
|
|---|---|---|
| Page(s) | 804 - 805 | |
| Section | Le Magazine : Nouvelles | |
| DOI | https://doi.org/10.1051/medsci/20021889804 | |
| Published online | 15 August 2002 | |
- Kurima K, Peters LM, Yang Y, et al. Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function. Nat Genet 2002; 30 : 277–83. [Google Scholar]
- Jain PK, Fukushima K, Deshmukh D, et al. A human recessive neurosensory non syndromic hearing impairement locus is a potential homologue of the murine deafness (dn) locus. Hum Mol Genet 1995; 4 : 2391–4. [Google Scholar]
- Van Camp G, Willems PJ, Smith RJH. Nonsyndromic hearing impairment : unparalleled heterogeneity. Am J Hum Genet 1997; 60 : 758–64. [Google Scholar]
- Vreugde S, Erven A, Kros CJ, et al. Beethoven, a mouse model for dominant progessive hearing loss DFNA36. Nat Genet 2002; 30 : 257–8. [Google Scholar]
- Kiernan AE, Zalzman M, Fuchs H, et al. Tailchaser (Tlc) : a new mouse mutation affecting bundle differenciation and hair survival. J Neurocytol 1999; 28 : 969–85. [Google Scholar]
Current usage metrics show cumulative count of Article Views (full-text article views including HTML views, PDF and ePub downloads, according to the available data) and Abstracts Views on Vision4Press platform.
Data correspond to usage on the plateform after 2015. The current usage metrics is available 48-96 hours after online publication and is updated daily on week days.
Initial download of the metrics may take a while.