Whole exome sequencing resolves complex phenotype and identifies CC2D2A mutations underlying non-syndromic rod-cone dystrophy

Published 2018 View Full Article

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Title
Whole exome sequencing resolves complex phenotype and identifies CC2D2A mutations underlying non-syndromic rod-cone dystrophy
Authors
Keywords
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Journal
CLINICAL GENETICS
Volume -, Issue -, Pages -
Publisher
Wiley
Online
2018-09-29
DOI
10.1111/cge.13453

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