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

82 Citations (Scopus)
Original languageEnglish (US)
JournalJournal of Medical Genetics
Volume40
Issue number5
StatePublished - May 2003

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DNA Mutational Analysis
Molecular Sequence Data
Audiology
Founder Effect
Consanguinity
Connexins
Hearing Loss
Gene Frequency
India
Amino Acid Sequence
Genotype
Phenotype
Mutation

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

Cite this

RamShankar, M., Girirajan, S., Dagan, O., Ravi Shankar, H. M., Jalvi, R., Rangasayee, R., ... Anand, A. (2003). Contribution of connexin26 (GJB2) mutations and founder effect to non-syndromic hearing loss in India. Journal of Medical Genetics, 40(5).

Contribution of connexin26 (GJB2) mutations and founder effect to non-syndromic hearing loss in India. / RamShankar, M.; Girirajan, S.; Dagan, O.; Ravi Shankar, H. M.; Jalvi, R.; Rangasayee, R.; Avraham, K. B.; Anand, A.

In: Journal of Medical Genetics, Vol. 40, No. 5, 05.2003.

Research output: Contribution to journalArticle

RamShankar, M, Girirajan, S, Dagan, O, Ravi Shankar, HM, Jalvi, R, Rangasayee, R, Avraham, KB & Anand, A 2003, 'Contribution of connexin26 (GJB2) mutations and founder effect to non-syndromic hearing loss in India.', Journal of Medical Genetics, vol. 40, no. 5.
RamShankar, M. ; Girirajan, S. ; Dagan, O. ; Ravi Shankar, H. M. ; Jalvi, R. ; Rangasayee, R. ; Avraham, K. B. ; Anand, A. / Contribution of connexin26 (GJB2) mutations and founder effect to non-syndromic hearing loss in India. In: Journal of Medical Genetics. 2003 ; Vol. 40, No. 5.
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