Mutation of Solute Carrier SLC16A12 Associates with a Syndrome Combining Juvenile Cataract with Microcornea and Renal Glucosuria

Title
Mutation of Solute Carrier SLC16A12 Associates with a Syndrome Combining Juvenile Cataract with Microcornea and Renal Glucosuria
Authors
Keywords
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Journal
AMERICAN JOURNAL OF HUMAN GENETICS
Volume 82, Issue 3, Pages 772-779
Publisher
Elsevier BV
Online
2008-03-04
DOI
10.1016/j.ajhg.2007.12.013

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