Homozygous loss-of-function mutation of theLEPREL1gene causes severe non-syndromic high myopia with early-onset cataract

Title
Homozygous loss-of-function mutation of theLEPREL1gene causes severe non-syndromic high myopia with early-onset cataract
Authors
Keywords
-
Journal
CLINICAL GENETICS
Volume 86, Issue 6, Pages 575-579
Publisher
Wiley
Online
2013-10-30
DOI
10.1111/cge.12309

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