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1 article related to "Efnb1 Mutation"

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Articles

Case Report

Published on 01 Sep 2020

Trio-Based Whole-Exome Sequencing Identifies a De novo EFNB1 Mutation as a Genetic Cause in Female Infant With Brain Anomaly and Developmental Delay

in Genetics of Common and Rare Diseases

Ji Yoon Han
Hyun Jeong Kim
Ja Hyun Jang
In Goo Lee
Joonhong Park

Frontiers in Pediatrics

doi 10.3389/fped.2020.00461

5,707 views
6 citations