Cha Gon Lee
7PUBLICATIONS
4CO-AUTHORS
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Publications (7)
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|Apr 10, 2024
KCNJ3 is a novel candidate gene for autosomal dominant pure hereditary spastic paraplegia identified using whole genome sequencing.Woong-Woo Lee, Cha Gon Lee, Chang-Seok Ki
|Jan 05, 2024
Novel In-Frame Deletion CNOT3 Variant in a Family With Intellectual Developmental Disorder With Speech Delay and Dysmorphic Facies.Cha Gon Lee, Hyun Jung Kim, Chang Ahn Seol
|Jul 27, 2023
Intracranial Vessel Wall Magnetic Resonance Imaging of Middle Cerebral Artery Dissection in Neurofibromatosis Type 1.Kyusik Kang, Cha Gon Lee, Byung-Kun Kim
|Dec 11, 2020
A Novel De Novo Heterozygous ARID1A Missense Variant Cluster in cis c.[5954C>G;6314C>T;6334C>T;6843G>C] causes a Coffin-Siris Syndrome.Cha Gon Lee, Chang-Seok Ki
|Sep 09, 2020
The first familial case of inherited intellectual developmental disorder with dysmorphic facies and behavioral abnormalities (IDDFBA) with a novel FBXO11 variant.Cha Gon Lee, Chang Ahn Seol, Chang-Seok Ki
|Jun 21, 2018
Multi-gene panel testing in Korean patients with common genetic generalized epilepsy syndromes.Cha Gon Lee, Jeehun Lee, Munhyang Lee
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