The Genetic Causes of Nonsyndromic Congenital Retinal Detachment: A Genetic and Phenotypic Study of Pakistani Families. [electronic resource]
Producer: 20170626Description: 1028-1036 p. digitalISSN:- 1552-5783
- Basic Helix-Loop-Helix Transcription Factors -- genetics
- Child
- Child, Preschool
- DNA Mutational Analysis
- Female
- Genotype
- Helix-Loop-Helix Motifs
- Humans
- Incidence
- Infant
- Male
- Mutation
- Pakistan -- epidemiology
- Pedigree
- Phenotype
- Polymorphism, Single Nucleotide
- Retina -- metabolism
- Retinal Diseases -- congenital
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Publication Type: Journal Article; Multicenter Study; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
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