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

Experimental and Molecular Medicine

Volumn 43, Issue 7, 2011, Pages 393-400

  Lee, Eun Ju ^a,b   Kim, Kwang Joong ^b   Kim, Han Na ^a   Bok, Jeong ^b   Jung, Sung Chul ^a   Kim, Eung Kweon ^c   Lee, Jong Young ^b   Kim, Hyung Lae ^a,d  

^a Ewha Womans University School of Medicine   (South Korea)

^b Korea National Institute of Health   (South Korea)

^c Yonsei University College of Medicine   (South Korea)

^d Korea Centers for Disease Control and Prevention   (South Korea)

Author keywords

Corneal dystrophies; Genomewide association study; Hereditary; Neurofibromin 2; Polymorphism; Single nucleotide; Transforming growth factor 1

Indexed keywords

NEUROLIGIN 1; TRANSFORMING GROWTH FACTOR BETA;

ARTICLE; AVELLINO CORNEA DYSTROPHY; CHROMOSOME 3Q; CHROMOSOME 5Q; CONTROLLED STUDY; CORNEA DYSTROPHY; FEMALE; GENE; GENE LOCUS; GENETIC HETEROGENEITY; GENETIC LINKAGE; GENOTYPE; GRANULAR CORNEA DYSTROPHY TYPE II; HEREDITY; HUMAN; LINKAGE ANALYSIS; MALE; PATHOPHYSIOLOGY; PHENOTYPIC VARIATION; SIMULATION; SINGLE NUCLEOTIDE POLYMORPHISM;

EID: 79960995379     PISSN: 12263613     EISSN: 20926413     Source Type: Journal    
DOI: 10.3858/emm.2011.43.7.043     Document Type: Article

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