GJB2 and GJB6 Genes: Molecular Study and Identification of Novel GJB2 Mutations in the Hearing-Impaired Argentinean Population
2010
Mutations in the GJB2 gene are responsible for more than half of all cases of recessive non-syndromic deafness. This article presents a mutation analysis of the GJB2
Keywords:
- Correction
- Source
- Cite
- Save
- Machine Reading By IdeaReader
40
References
19
Citations
NaN
KQI