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DGAT2Mutation in a Family with Autosomal-Dominant Early-Onset Axonal Charcot-Marie-Tooth Disease

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Year: 2016
Type: article
Source: Human Mutation
DOI: 10.1002/humu.22959
Authors: Young Bin Hong, Junghee Kang, Ji Hyun Kim, Jinho Lee, Geon Kwak, Young Se Hyun, Soo Hyun Nam, Hyun Dae Hong, Yu-Ri Choi, Sung-Chul Jung, Heasoo Koo, Ji Eun Lee, Byung-Ok Choi, Ki Wha Chung
Institutions: Samsung Medical Center, Sungkyunkwan University, Kongju National University, Ewha Womans University, Ewha Womans University Mokdong Hospital
Language: English

Topic: Hereditary Neurological Disorders
Subfield: Cellular and Molecular Neuroscience
Field: Neuroscience
Domain: Life Sciences
SDG: Good health and well-being

Open Access status: closed

Funder: National Research Foundation
Awards: G4307710479, G6167241666, G7213423815
OpenAlex ID: W2275708487
FWCI: 2.171
Cites: 35
Cited by: 50
Related to: 10
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