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

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

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

Authors: Park H.J.; Lee J.H.; Shin H.Y.; Kim S.M.; Choi Y.-C.

Ewha Authors: 박형준

SCOPUS Author ID: 박형준

Issue Date: 2016

Journal Title: Journal of Clinical Neurology (Korea)

ISSN: 1738-6586

Citation: Journal of Clinical Neurology (Korea) vol. 12, no. 1, pp. 121 - 122

Publisher: Korean Neurological Association

Indexed: SCIE; SCOPUS; KCI

Document Type: Letter

Abstract: [No abstract available]

DOI: 10.3988/jcn.2016.12.1.121

Appears in Collections:: 의료원 > 의료원 > Journal papers

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