Mutation of FOXC1 and PITX2 induces cerebral small-vessel disease.
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Overview
publication date
- September 24, 2014
has subject area
- Animals
- Cerebral Hemorrhage
- Cerebral Small Vessel Diseases
- Codon, Nonsense
- Forkhead Transcription Factors
- Genetic Predisposition to Disease
- Genome-Wide Association Study
- Homeobox Protein PITX2
- Homeodomain Proteins
- Humans
- Leukoencephalopathies
- Linkage Disequilibrium
- Mutation, Missense
- Platelet-Derived Growth Factor
- Polymorphism, Single Nucleotide
- Quantitative Trait Loci
- Signal Transduction
- Transcription Factors
- Zebrafish