EPS8L2 is a new causal gene for childhood onset autosomal recessive progressive hearing loss.
| Autor: | Dahmani, Malika1, Ammar-Khodja, Fatima1, Bonnet, Crystel2,3,4, Lefèvre, Gaelle M.2,3,4, Hardelin, Jean-Pierre3,4,5, Ibrahim, Hassina6, Mallek, Zahia7, Petit, Christine2,3,4,8 christine.petit@pasteur.fr |
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| Zdroj: | Orphanet Journal of Rare Diseases. Aug2015, Vol. 10 Issue 1, p1-5. 5p. |
| Databáze: | Academic Search Ultimate |
| Externí odkaz: |
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