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

All Science Journal Classification (ASJC) codes

Genetics
Genetics(clinical)

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10.1136/jmg.40.5.e68

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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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AU - Girirajan, S.

AU - Dagan, O.

AU - Ravi Shankar, H. M.

AU - Jalvi, R.

AU - Rangasayee, R.

AU - Avraham, K. B.

AU - Anand, A.

PY - 2003/5

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SN - 0022-2593

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JF - Journal of medical genetics

IS - 5

ER -

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

All Science Journal Classification (ASJC) codes

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