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Exome sequencing identifies a recessive PIGN splice site mutation as a cause of syndromic Congenital Diaphragmatic Hernia

✍ Scribed by Brady, P.D.; Moerman, Philippe; De Catte, Luc; Deprest, J.; Devriendt, K.; Vermeesch, J.R.

Book ID: 124126427
Publisher: Elsevier Science
Year: 2014
Tongue: English
Weight: 621 KB
Volume: 57
Category: Article
ISSN: 1769-7212
DOI: 10.1016/j.ejmg.2014.05.001

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