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 journalArticlepeer-review

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

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

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