New intragenic deletions in the Phex gene clarify X-linked hypophosphatemia-related abnormalities in mice. [electronic resource]
Producer: 20041019Description: 151-61 p. digitalISSN:- 0938-8990
- Absorptiometry, Photon
- Animals
- Base Sequence -- genetics
- Blotting, Southern
- Body Composition
- Body Weights and Measures
- Bone Density
- Cochlea -- abnormalities
- DNA Primers
- Disease Models, Animal
- Evoked Potentials, Auditory, Brain Stem
- Genetic Diseases, X-Linked -- genetics
- Histological Techniques
- Hypophosphatemia -- genetics
- Male
- Mice -- abnormalities
- Mice, Inbred C57BL
- PHEX Phosphate Regulating Neutral Endopeptidase
- Phenotype
- Proteins -- genetics
- Reverse Transcriptase Polymerase Chain Reaction
- Sequence Analysis, DNA
- Sequence Deletion -- genetics
- Skull -- abnormalities
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Publication Type: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
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