Associated Papers
Whole-exome sequencing in a Japanese multiplex family identifies new susceptibility genes for intracranial aneurysms.
Maegawa T et al.
Plos One, 2022
A case report of de novo missense FOXP1 mutation in a non-Caucasian patient with global developmental delay and severe speech impairment.
Song H et al.
Clinical Case Reports, 2015
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