Prenatal molecular diagnosis and carrier detection of Duchenne muscular dystrophy in Korea-Reference-Cited by-同舟云学术

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Prenatal molecular diagnosis and carrier detection of Duchenne muscular dystrophy in Korea

Published:2020-06-30 Issue:1 Volume:17 Page:27-33
ISSN:1226-1769
Container-title:Journal of Genetic Medicine
language:en
Short-container-title:J Genet Med

Author:

Kang Min Ji¹²^ORCID,Seong Moon-Woo³^ORCID,Cho Sung Im³^ORCID,Park Joong Shin¹^ORCID,Jun Jong Kwan¹⁴^ORCID,Park Sung Sup³^ORCID

Affiliation:

1. Department of Obstetrics and Gynecology, Seoul National University College of Medicine, Seoul, Korea

2. Department of Obstetrics and Gynecology, Gimcheon Jeil Hospital, Gimcheon, Korea

3. Department of Laboratory Medicine, Seoul National University College of Medicine, Seoul, Korea

4. Institute of Reproductive Medicine and Population, Medical Research Center, Seoul National University College of Medicine, Seoul, Korea

Funder

Korea Health Industry Development Institute

Ministry of Health and Welfare

Publisher

Korean Society of Medical Genetics

Subject

General Medicine

Link

http://pdf.medrang.co.kr/JGM/2020/017/JGM017-01-05.pdf

Reference22 articles.

1. The muscular dystrophies

2. 195th ENMC International Workshop: Newborn screening for Duchenne muscular dystrophy 14–16th December, 2012, Naarden, The Netherlands

3. Dystrophin: The protein product of the duchenne muscular dystrophy locus

4. Linkage relationship of a cloned DNA sequence on the short arm of the X chromosome to Duchenne muscular dystrophy

5. Dystrophin and mutations: one gene, several proteins, multiple phenotypes

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