Connexin 26 (GJB2) mutation in an Argentinean patient with keratitis-ichthyosis-deafness (KID) syndrome: a case report
Crossref DOI link: https://0-doi-org.brum.beds.ac.uk/10.1186/s12881-016-0298-y
Published Online: 2016-05-04
Published Print: 2016-12
Update policy: https://0-doi-org.brum.beds.ac.uk/10.1007/springer_crossmark_policy
Dalamón, Viviana Karina
Buonfiglio, Paula
Larralde, Margarita
Craig, Patricio
Lotersztein, Vanesa
Choate, Keith
Pallares, Norma
Diamante, Vicente
Elgoyhen, Ana Belén
Funding for this research was provided by:
ANPCyT (2012 Number 2133)