Heterozygous and homozygous mutations in PITX3 in a large Lebanese family with posterior polar cataracts and neurodevelopmental abnormalities. [electronic resource]
Producer: 20060427Description: 1274-80 p. digitalISSN:- 0146-0404
- Cataract -- genetics
- Chromosomes, Human, Pair 10 -- genetics
- Consanguinity
- DNA Mutational Analysis
- Female
- Genetic Linkage
- Haplotypes
- Heterozygote
- Homeodomain Proteins -- genetics
- Homozygote
- Humans
- Lebanon
- Lod Score
- Male
- Microphthalmos -- genetics
- Mutation
- Nervous System Diseases -- genetics
- Pedigree
- Transcription Factors -- genetics
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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