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CTNND2 is a genetic variant for high myopia.

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Bibliographic Details
Title: CTNND2 is a genetic variant for high myopia.
Authors: SAW, SM1 (AUTHOR), FAN, Q1 (AUTHOR), YOSHIMURA, N2 (AUTHOR), KHOR, CC3 (AUTHOR), TAI, ES4 (AUTHOR), GOH, LK5 (AUTHOR), YOUNG, T6 (AUTHOR), LI, YL7 (AUTHOR)
Source: Acta Ophthalmologica (1755375X). Sep2011 Supplement S248, Vol. 89, p0-0. 1p.
Database: Academic Search Ultimate
Description
ISSN:1755375X
DOI:10.1111/j.1755-3768.2011.2222.x