Novel Mutations in the Connexin 26 Gene (GJB2) That Cause Autosomal Recessive (DFNB1) Hearing Loss - Concepedia

Concepedia

Publication | Open Access

Novel Mutations in the Connexin 26 Gene (GJB2) That Cause Autosomal Recessive (DFNB1) Hearing Loss

DOI Full Paper Access

505

Citations

16

References

1998

Year

Philip M. Kelley, David J. Harris, B.C. Comer, James W. Askew, Trent Fowler, S. D. Smith, William J. Kimberling

The American Journal of Human Genetics

Developmental BiologyMendelian DisorderGenetic DisorderGeneticsAudiologyNovel MutationsAuditory PhysiologyAuditory ResearchAuditory ScienceHuman HearingArtsMedicineConnexin 26Auditory SystemHearing Loss

References

	Year	Citations

Page 1

Page 1