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

doi:10.1136/jmg.40.5.e68

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 journal › Article › peer-review

Original language	English (US)
Pages (from-to)	e68
Journal	Journal of medical genetics
Volume	40
Issue number	5
DOIs	https://doi.org/10.1136/jmg.40.5.e68
State	Published - May 2003

ASJC Scopus subject areas

Genetics
Genetics(clinical)

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

author = "M. RamShankar and S. Girirajan and O. Dagan and {Ravi Shankar}, {H. M.} and R. Jalvi and R. Rangasayee and Avraham, {K. B.} and A. Anand",

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

ASJC Scopus subject areas

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