Novel SGCE gene mutation in a Korean patient with myoclonus-dystonia with unique phenotype mimicking Moya-Moya disease [4]

Joo Chung Eun; Yong Lee Won; Ji Youn Kim; Jong Hun Kim; Gyeong Moon Kim; Seok Ki Chang; In Suk Kim

doi:10.1002/mds.21093

Novel SGCE gene mutation in a Korean patient with myoclonus-dystonia with unique phenotype mimicking Moya-Moya disease [4]

Joo Chung Eun
, Yong Lee Won
, Ji Youn Kim
, Jong Hun Kim
, Gyeong Moon Kim
, Seok Ki Chang
, In Suk Kim

Department of Neurology

Sungkyunkwan University

Research output: Contribution to journal › Letter › peer-review

13 Scopus citations

Original language	English
Pages (from-to)	1206-1207
Number of pages	2
Journal	Movement Disorders
Volume	22
Issue number	8
DOIs	https://doi.org/10.1002/mds.21093
State	Published - 15 Jun 2007

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

SDG 3 Good Health and Well-being

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10.1002/mds.21093

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@article{362173e5686544138b17ced68446ea68,

title = "Novel SGCE gene mutation in a Korean patient with myoclonus-dystonia with unique phenotype mimicking Moya-Moya disease [4]",

author = "Eun, \{Joo Chung\} and Won, \{Yong Lee\} and Kim, \{Ji Youn\} and Kim, \{Jong Hun\} and Kim, \{Gyeong Moon\} and Chang, \{Seok Ki\} and Kim, \{In Suk\}",

year = "2007",

month = jun,

day = "15",

doi = "10.1002/mds.21093",

language = "English",

volume = "22",

pages = "1206--1207",

journal = "Movement Disorders",

issn = "0885-3185",

publisher = "John Wiley \& Sons Inc.",

number = "8",

}

TY - JOUR

T1 - Novel SGCE gene mutation in a Korean patient with myoclonus-dystonia with unique phenotype mimicking Moya-Moya disease [4]

AU - Eun, Joo Chung

AU - Won, Yong Lee

AU - Kim, Ji Youn

AU - Kim, Jong Hun

AU - Kim, Gyeong Moon

AU - Chang, Seok Ki

AU - Kim, In Suk

PY - 2007/6/15

Y1 - 2007/6/15

UR - https://www.scopus.com/pages/publications/34447506221

U2 - 10.1002/mds.21093

DO - 10.1002/mds.21093

M3 - Letter

C2 - 17394247

AN - SCOPUS:34447506221

SN - 0885-3185

VL - 22

SP - 1206

EP - 1207

JO - Movement Disorders

JF - Movement Disorders

IS - 8

ER -

Novel SGCE gene mutation in a Korean patient with myoclonus-dystonia with unique phenotype mimicking Moya-Moya disease [4]

UN SDGs

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