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Human Molecular Genetics, ISSN 0964-6906, 10/1996, Volume 5, Issue 10, pp. 1667 - 1672
Schnyder's crystalline corneal dystrophy (SCCD) is an autosomal dominant eye disease characterized by a bilateral clouding of the central cornea, arcus... 
LOCALIZATION | HUMAN GENOME | BIOCHEMISTRY & MOLECULAR BIOLOGY | MUTATION | DISEASE | GENETICS & HEREDITY | LINKAGE ANALYSIS | ARCUS | LIPOPROTEIN-LIPASE | FAMILY | Haplotypes | Corneal Dystrophies, Hereditary - genetics | Chromosome Mapping | Chromosomes, Human, Pair 1 | Pedigree | Humans | Index Medicus
Journal Article
Der Ophthalmologe, ISSN 0941-293X, 11/2003, Volume 100, Issue 11, pp. 979 - 983
Die seltene Schnydersche kristalline Hornhautdystrophie (SCCD) wird autosomal-dominant vererbt und kann mit einer Hyperlipoproteinämie vergesellschaftet sein.... 
Medicine | Linkage study | Chromosome 1p34.1-p36 | Schnydersche kristalline Hornhautdystrophie | Genetische Kopplungsuntersuchungen | Chromosom 1p34.1–p36 | Hyperlipoproteinemia | Hyperlipoproteinämie | Schnyder's crystalline corneal dystrophy
Journal Article
American Journal of Medical Genetics Part A, ISSN 1552-4825, 02/2008, Volume 146A, Issue 3, pp. 271 - 283
Journal Article
American Journal of Medical Genetics Part A, ISSN 1552-4825, 04/2008, Volume 146A, Issue 7, pp. 952 - 964
Schnyder crystalline corneal dystrophy (SCCD) is a rare autosomal dominant disease characterized by progressive corneal opacification resulting from abnormal... 
UBIAD1 | Schnyder crystalline corneal dystrophy | cornea | corneal dystrophy | phospholipids | prenyltransferase | hypercholesterolemia | ocular | eye | HDL | LDL | cholesterol | Schnyder corneal dystrophy | genetic disease | LOCALIZATION | ESCHERICHIA-COLI | LOCUS | APOLIPOPROTEIN-E | PREDICTION | HYPERLIPOPROTEINEMIA | SEQUENCE | GENETICS & HEREDITY | MUTATIONS | CHROMOSOME 1P34.1-P36
Journal Article
PLoS ONE, ISSN 1932-6203, 08/2007, Volume 2, Issue 8, pp. e685 - e685
Journal Article
Human Genetics, ISSN 0340-6717, 05/2004, Volume 114, Issue 6, pp. 594 - 600
Schnyder's crystalline corneal dystrophy (SCCD) is a rare autosomal dominant eye disease with a spectrum of clinical manifestations that may include bilateral... 
CONFOCAL MICROSCOPY | PROTEIN | GENE | GENETICS & HEREDITY | Founder Effect | Haplotypes - genetics | Pedigree | Humans | Corneal Dystrophies, Hereditary - genetics | Genotype | Chromosome Mapping | Chromosomes, Human, Pair 1 - genetics | Microsatellite Repeats | Index Medicus
Journal Article
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