The mottled mouse as a model for human Menkes disease: identification of mutations in the Atp7a gene. [electronic resource]
Producer: 19970515Description: 425-33 p. digitalISSN:- 0964-6906
- Adenosine Triphosphatases -- genetics
- Animals
- Carrier Proteins -- genetics
- Cation Transport Proteins
- Copper -- metabolism
- Copper-Transporting ATPases
- DNA Mutational Analysis
- DNA Primers -- chemistry
- Disease Models, Animal
- Electrophoresis, Polyacrylamide Gel
- Embryo, Mammalian -- metabolism
- Fluorescence
- Heterozygote
- Humans
- Menkes Kinky Hair Syndrome -- genetics
- Mice
- Mutation
- Phenotype
- Polymorphism, Genetic
- RNA, Messenger -- genetics
- Recombinant Fusion Proteins
- Sequence Analysis
- Sequence Deletion
- Transcription, Genetic
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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