Concepedia

Publication | Open Access

Connexin 26 (GJB2) mutation in an Argentinean patient with keratitis-ichthyosis-deafness (KID) syndrome: a case report

DOIFull Paper Access

14

Citations

34

References

2016

Year

Viviana Dalamón, Paula I. Buonfiglio, Margarita Larralde, Patricio O. Craig, Vanesa Lotersztein, Keith A. Choate, Norma Pallares, Vicente Diamante, Ana Belén Elgoyhen
BMC Medical Genetics

References

YearCitations

Page 1