Wieben et al., 2014 - Google Patents
Comprehensive assessment of genetic variants within TCF4 in Fuchs' endothelial corneal dystrophyWieben et al., 2014
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- 8013178648501479727
- Author
- Wieben E
- Aleff R
- Eckloff B
- Atkinson E
- Baheti S
- Middha S
- Brown W
- Patel S
- Kocher J
- Baratz K
- Publication year
- Publication venue
- Investigative ophthalmology & visual science
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Snippet
Purpose.: The single nucleotide variant (SNV), rs613872, in the transcription factor 4 (TCF4) gene was previously found to be strongly associated (P= 6× 10− 26) with Fuchs' endothelial corneal dystrophy (FECD). Subsequently, an intronic expansion of the repeating …
- 201000001925 Fuchs' endothelial dystrophy 0 title abstract description 82
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- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or micro-organisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or micro-organisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
- C12Q1/6876—Hybridisation probes
- C12Q1/6883—Hybridisation probes for diseases caused by alterations of genetic material
- C12Q1/6886—Hybridisation probes for diseases caused by alterations of genetic material for cancer
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- C12Q2600/00—Oligonucleotides characterized by their use
- C12Q2600/156—Polymorphic or mutational markers
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- C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
- C12N15/09—Recombinant DNA-technology
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- C12Q2600/00—Oligonucleotides characterized by their use
- C12Q2600/172—Haplotypes
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