Isolation and characterization of a calcium channel gene, Cacna1f, the murine orthologue of the gene for incomplete X-linked congenital stationary night blindness. [electronic resource]
Producer: 20000911Description: 324-7 p. digitalISSN:- 0888-7543
- Animals
- Calcium Channels -- genetics
- Calcium Channels, L-Type -- genetics
- DNA Primers
- Eye -- metabolism
- Humans
- In Situ Hybridization
- Mice
- Molecular Sequence Data
- Night Blindness -- genetics
- Organ Specificity
- Physical Chromosome Mapping
- RNA, Messenger -- biosynthesis
- Retina -- metabolism
- Reverse Transcriptase Polymerase Chain Reaction
- Sequence Analysis, DNA
- Sequence Homology, Nucleic Acid
- X Chromosome -- genetics
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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