Contribution of connexin26 (GJB2) mutations and founder effect to non-syndromic hearing loss in India.

M. RamShankar, S. Girirajan, O. Dagan, H. M. Ravi Shankar, R. Jalvi, R. Rangasayee, K. B. Avraham, A. Anand

Research output: Contribution to journalArticle

86 Scopus citations
Original languageEnglish (US)
Pages (from-to)e68
JournalJournal of medical genetics
Volume40
Issue number5
DOIs
StatePublished - May 2003

All Science Journal Classification (ASJC) codes

  • Genetics
  • Genetics(clinical)

Cite this

RamShankar, M., Girirajan, S., Dagan, O., Ravi Shankar, H. M., Jalvi, R., Rangasayee, R., Avraham, K. B., & Anand, A. (2003). Contribution of connexin26 (GJB2) mutations and founder effect to non-syndromic hearing loss in India. Journal of medical genetics, 40(5), e68. https://doi.org/10.1136/jmg.40.5.e68