EPS8L2 is a new causal gene for childhood onset autosomal recessive progressive hearing loss
Crossref DOI link: https://doi.org/10.1186/s13023-015-0316-8
Published Online: 2015-08-19
Published Print: 2015-12
Update policy: https://doi.org/10.1007/springer_crossmark_policy
Dahmani, Malika
Ammar-Khodja, Fatima
Bonnet, Crystel
Lefèvre, Gaelle M.
Hardelin, Jean-Pierre
Ibrahim, Hassina
Mallek, Zahia
Petit, Christine