Connexin 26 (GJB2) mutations as a cause of the KID syndrome with hearing loss - Concepedia

Concepedia

Publication | Closed Access

Connexin 26 (GJB2) mutations as a cause of the KID syndrome with hearing loss

38

Citations

22

References

2010

Year

Alessandro Terrinoni, Andrea Codispoti, Valeria Serra, Ernesto Bruno, Biagio Didona, Mauro Paradisi, Steven Paul Nisticò, Elena Campione, Bianca Napolitano, Laura Diluvio,

Biochemical and Biophysical Research Communications

Developmental BiologyKid SyndromePediatric OtolaryngologyGenetic DisorderAudiologyPediatricsPathologyCochlear DevelopmentHuman HearingArtsMedicineConnexin 26Hearing Loss

References

	Year	Citations

Page 1

Page 1