P657: Structural variants identified by short-read genome sequencing solves missing heritability in retinal dystrophies

Bibliographic Details
Main Authors:	Ehsan Ullah, Amelia Naik, Chelsea Bender, Delphine Blain, Laryssa Huryn, Robert Hufnagel, Bin Guan
Format:	Article
Language:	English
Published:	Elsevier 2024-01-01
Series:	Genetics in Medicine Open
Online Access:	http://www.sciencedirect.com/science/article/pii/S2949774424007088

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