[Type I lattice corneal dystrophy. Clinical and molecular genetic study of a large family].
Meins, M
[Type I lattice corneal dystrophy. Clinical and molecular genetic study of a large family]. [electronic resource] - Klinische Monatsblatter fur Augenheilkunde Mar 1998 - 154-8 p. digital
Publication Type: Journal Article
0023-2165
10.1055/s-2008-1034852 doi
Adult
Aged
Chromosome Aberrations--genetics
Chromosome Disorders
Chromosomes, Human, Pair 5
Corneal Dystrophies, Hereditary--classification
DNA Mutational Analysis
DNA, Complementary--genetics
Extracellular Matrix Proteins--genetics
Eye Proteins--genetics
Female
Genes, Dominant--genetics
Genetic Carrier Screening
Humans
Male
Middle Aged
Pedigree
Polymerase Chain Reaction
RNA, Messenger--genetics
[Type I lattice corneal dystrophy. Clinical and molecular genetic study of a large family]. [electronic resource] - Klinische Monatsblatter fur Augenheilkunde Mar 1998 - 154-8 p. digital
Publication Type: Journal Article
0023-2165
10.1055/s-2008-1034852 doi
Adult
Aged
Chromosome Aberrations--genetics
Chromosome Disorders
Chromosomes, Human, Pair 5
Corneal Dystrophies, Hereditary--classification
DNA Mutational Analysis
DNA, Complementary--genetics
Extracellular Matrix Proteins--genetics
Eye Proteins--genetics
Female
Genes, Dominant--genetics
Genetic Carrier Screening
Humans
Male
Middle Aged
Pedigree
Polymerase Chain Reaction
RNA, Messenger--genetics