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Cha Gon Lee

7PUBLICATIONS

4CO-AUTHORS

Neurology and neuromuscular diseasesEpigenetics (incl. genome methylation and epigenomics)NeurogeneticsDevelopmental genetics (incl. sex determination)Gene mapping

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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 <i>CNOT3</i> 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 <i>De Novo</i> Heterozygous <i>ARID1A</i> Missense Variant Cluster in <i>cis</i> 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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Frequent Collaborators

1 joint publications

Jeehun Lee

1 joint publications

Chang-Seok Ki

1 joint publications

Kyusik Kang

1 joint publications

Byung-Kun Kim

Frequent Collaborators

1 joint publications

Jeehun Lee

1 joint publications

Chang-Seok Ki

1 joint publications

Kyusik Kang

1 joint publications

Byung-Kun Kim

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