Trio-Based Whole-Exome Sequencing Identifies a De novo EFB1 Mutation as a Genetic Cause in Female Infant With Brain Anomaly and Developmental Delay

Joonhong Park

Trio-Based Whole-Exome Sequencing Identifies a De novo EFB1 Mutation as a Genetic Cause in Female Infant With Brain Anomaly and Developmental Delay

Joonhong Park

Department of Medicine

Research output: Contribution to journal › Journal article › peer-review

Original language	Korean
Journal	Frontiers in Pediatrics
State	Published - 2020.09.1

Cite this

@article{1352fe00aa954d1283cf7968c1218b23,

title = "Trio-Based Whole-Exome Sequencing Identifies a De novo EFB1 Mutation as a Genetic Cause in Female Infant With Brain Anomaly and Developmental Delay",

author = "Joonhong Park",

year = "2020",

month = sep,

day = "1",

language = "Korean",

journal = "Frontiers in Pediatrics",

issn = "2296-2360",

}