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CTNND2 is a genetic variant for high myopia.

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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
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  Availability: 0
Header DbId: asn
DbLabel: Academic Search Ultimate
An: 157963817
AccessLevel: 2
PubType: Academic Journal
PubTypeId: academicJournal
PreciseRelevancyScore: 0
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  Data: CTNND2 is a genetic variant for high myopia.
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RecordInfo BibRecord:
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        Value: 10.1111/j.1755-3768.2011.2222.x
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      – Code: eng
        Text: English
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      – TitleFull: CTNND2 is a genetic variant for high myopia.
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            NameFull: SAW, SM
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              Text: Sep2011 Supplement S248
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              Y: 2011
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