Evaluating the association of bone morphogenetic protein 4-V152A and SIX homeobox 6-H141N polymorphisms with congenital cataract and microphthalmia in Western Indian population. [electronic resource]
Producer: 20191015Description: 86-91 p. digitalISSN:- 0972-2823
- Asian People -- genetics
- Bone Morphogenetic Protein 4 -- genetics
- Case-Control Studies
- Cataract -- congenital
- Child
- Child, Preschool
- Cohort Studies
- Female
- Genes, Homeobox -- genetics
- Genetic Predisposition to Disease
- Genotype
- Humans
- Male
- Microphthalmos -- genetics
- Mutation -- genetics
- Polymorphism, Single Nucleotide -- genetics
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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