A mutation in Tpst2 encoding tyrosylprotein sulfotransferase causes dwarfism associated with hypothyroidism. [electronic resource]
Producer: 20070815Description: 1713-21 p. digitalISSN:- 0888-8809
- Amino Acid Sequence
- Animals
- Base Sequence
- Congenital Hypothyroidism -- complications
- DNA Primers -- genetics
- Dwarfism -- complications
- Female
- Genetic Complementation Test
- Male
- Mice
- Mice, Inbred C57BL
- Mice, Mutant Strains
- Mice, Transgenic
- Molecular Sequence Data
- Mutation, Missense
- Phenotype
- Protein Processing, Post-Translational
- Receptors, Thyrotropin -- metabolism
- Sequence Homology, Amino Acid
- Signal Transduction
- Substrate Specificity
- Sulfotransferases -- deficiency
- Thyrotropin -- metabolism
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Publication Type: Journal Article
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