Exome sequencing identifies a recessive PIGN splice site mutation as a cause of syndromic congenital diaphragmatic hernia. (Q34421014)
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scientific article
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Exome sequencing identifies a recessive PIGN splice site mutation as a cause of syndromic congenital diaphragmatic hernia. |
scientific article |
Statements
Exome sequencing identifies a recessive PIGN splice site mutation as a cause of syndromic congenital diaphragmatic hernia (English)
P D Brady
Philippe Moerman
Luc De Catte
K Devriendt