Where are the missing gene defects in inherited retinal disorders? Intronic and synonymous variants contribute at least to 4% of CACNA1F ‐mediated inherited retinal disorders
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Title
Where are the missing gene defects in inherited retinal disorders? Intronic and synonymous variants contribute at least to 4% of
CACNA1F
‐mediated inherited retinal disorders
Authors
Keywords
-
Journal
HUMAN MUTATION
Volume -, Issue -, Pages -
Publisher
Wiley
Online
2019-03-02
DOI
10.1002/humu.23735
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