Cha Gon Lee

7PUBLICATIONS
4CO-AUTHORS
Neurology and neuromuscular diseasesEpigenetics (incl. genome methylation and epigenomics)Developmental genetics (incl. sex determination)Gene mappingVision science
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Publications (7)

|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

|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

|Jan 12, 2017
Identification of a Novel Mutation in BRD4 that Causes Autosomal Dominant Syndromic Congenital Cataracts Associated with Other Neuro-Skeletal Anomalies.

Hyun-Seok Jin, Jeonhyun Kim, Woori Kwak

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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