First identification of compound heterozygous FKRP mutations in a Korean patient with limb-girdle muscular dystrophy

Hyung Jun Park; Jung Hwan Lee; Ha Young Shin; Seung Min Kim; Ji Hyun Lee; Young Chul Choi

doi:10.3988/jcn.2016.12.1.121

First identification of compound heterozygous FKRP mutations in a Korean patient with limb-girdle muscular dystrophy

Hyung Jun Park, Jung Hwan Lee, Ha Young Shin, Seung Min Kim, Ji Hyun Lee, Young Chul Choi

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

3 Citations (Scopus)

Original language	English
Pages (from-to)	121-122
Number of pages	2
Journal	Journal of Clinical Neurology (Korea)
Volume	12
Issue number	1
DOIs	https://doi.org/10.3988/jcn.2016.12.1.121
Publication status	Published - Jan 2016

Access to Document

10.3988/jcn.2016.12.1.121

Cite this

@article{f7b910e4b46c4427926f8675c8cc96bd,

title = "First identification of compound heterozygous FKRP mutations in a Korean patient with limb-girdle muscular dystrophy",

author = "Park, {Hyung Jun} and Lee, {Jung Hwan} and Shin, {Ha Young} and Kim, {Seung Min} and Lee, {Ji Hyun} and Choi, {Young Chul}",

year = "2016",

month = jan,

doi = "10.3988/jcn.2016.12.1.121",

language = "English",

volume = "12",

pages = "121--122",

journal = "Journal of Clinical Neurology (Korea)",

issn = "1738-6586",

publisher = "Korean Neurological Association",

number = "1",

}

TY - JOUR

T1 - First identification of compound heterozygous FKRP mutations in a Korean patient with limb-girdle muscular dystrophy

AU - Park, Hyung Jun

AU - Lee, Jung Hwan

AU - Shin, Ha Young

AU - Kim, Seung Min

AU - Lee, Ji Hyun

AU - Choi, Young Chul

PY - 2016/1

Y1 - 2016/1

UR - http://www.scopus.com/inward/record.url?scp=84954357448&partnerID=8YFLogxK

U2 - 10.3988/jcn.2016.12.1.121

DO - 10.3988/jcn.2016.12.1.121

M3 - Letter

AN - SCOPUS:84954357448

SN - 1738-6586

VL - 12

SP - 121

EP - 122

JO - Journal of Clinical Neurology (Korea)

JF - Journal of Clinical Neurology (Korea)

IS - 1

ER -

First identification of compound heterozygous FKRP mutations in a Korean patient with limb-girdle muscular dystrophy

Access to Document

Other files and links

Cite this