Genome-wide scan of granular corneal dystrophy, type II: confirmation of chromosome 5q31 and identification of new co-segregated loci on chromosome 3q26.3-Reference-Cited by-同舟云学术

Genome-wide scan of granular corneal dystrophy, type II: confirmation of chromosome 5q31 and identification of new co-segregated loci on chromosome 3q26.3

Published:2011 Issue:7 Volume:43 Page:393
ISSN:1226-3613
Container-title:Experimental and Molecular Medicine
language:en
Short-container-title:Exp Mol Med

Author:

Lee Eun-Ju¹²,Kim Kwang Joong²,Kim Han-Na¹,Bok Jeong²,Jung Sung-Chul¹,Kim Eung Kweon³,Lee Jong-Young²,Kim Hyung-Lae¹⁴

Affiliation:

1. Department of Biochemistry, School of Medicine, Ewha Womans University, Seoul 158-710, Korea.

2. Division of Structural and Functional Genomics, Center for Genome Science, Korea National Institute of Health, Osong 363-951, Korea.

3. Corneal Dystrophy Research Institute, Department of Ophthalmology, Yonsei University College of Medicine, Seoul 120-752, Korea.

4. National Institute of Health, Korea Centers for Disease, Control and Prevention, Osong 363-951, Korea.

Publisher

Springer Science and Business Media LLC

Subject

Clinical Biochemistry,Molecular Biology,Molecular Medicine,Biochemistry

Reference28 articles.

1. Linkage Disequilibrium Inflates Type I Error Rates in Multipoint Linkage Analysis when Parental Genotypes Are Missing

3. Differentiation of human neural stem cells into retinal cells

4. Ignoring Linkage Disequilibrium among Tightly Linked Markers Induces False-Positive Evidence of Linkage for Affected Sib Pair Analysis

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