Missense mutation outside the forkhead domain of FOXL2 causes a severe form of BPES type II. [electronic resource]
Producer: 20120717Description: 211-8 p. digitalISSN:- 1090-0535
- Base Sequence
- Blepharophimosis -- genetics
- DNA Mutational Analysis
- Female
- Forkhead Box Protein L2
- Forkhead Transcription Factors -- genetics
- Genes, Dominant
- Genetic Linkage
- Genotype
- Heterozygote
- Humans
- Iran
- Male
- Molecular Sequence Data
- Mutation, Missense
- Pedigree
- Phenotype
- Protein Structure, Tertiary
- Severity of Illness Index
- Skin Abnormalities -- genetics
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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