A 5-bp deletion in ELOVL4 is associated with two related forms of autosomal dominant macular dystrophy
Journal Article
Overview
publication date
- January 1, 2001
has subject area
- Animals
- Biochemical Phenomena - Amino Acid Sequence
- Biochemical Phenomena - Base Sequence
- Cellular Structures - Chromosomes, Human, Pair 6
- Chromosome Mapping
- Cloning, Molecular
- DNA Mutational Analysis
- Diagnostic Techniques and Procedures - In Situ Hybridization
- Diagnostic Techniques and Procedures - In Situ Hybridization
- Exons
- Eye Proteins
- Female
- Gene Components - Introns
- Genes - Genes, Dominant
- Genetic Structures - Base Sequence
- Genetic Structures - Chromosomes, Human, Pair 6
- Genetic Techniques - In Situ Hybridization
- Genome Components - Introns
- Humans
- Inheritance Patterns - Genes, Dominant
- Investigative Techniques - In Situ Hybridization
- Investigative Techniques - In Situ Hybridization
- Lod Score
- Macaca mulatta
- Macular Degeneration
- Male
- Membrane Proteins
- Mice
- Molecular Sequence Data
- Molecular Sequence Data - Amino Acid Sequence
- Molecular Sequence Data - Base Sequence
- Mutagenesis - Sequence Deletion
- Mutation - Sequence Deletion
- Pedigree
- RNA, Messenger
- Retina
- Sequence Alignment
has restriction
- closed
Date in CU Experts
- September 3, 2013 3:18 AM
Full Author List
- Zhang K; Kniazeva M; Han M; Li W; Yu ZY; Yang ZL; Li Y; Metzker ML; Allikmets R; Zack DJ
author count
- 20
citation count
- 344
published in
- Nature Genetics Journal
Other Profiles
International Standard Serial Number (ISSN)
- 1061-4036
Digital Object Identifier (DOI)
Additional Document Info
start page
- 89
end page
- 93
volume
- 27
issue
- 1