A mutation in Tpst2 encoding tyrosylprotein sulfotransferase causes dwarfism associated with hypothyroidism.

Sasaki, Nobuya

A mutation in Tpst2 encoding tyrosylprotein sulfotransferase causes dwarfism associated with hypothyroidism. [electronic resource] - Molecular endocrinology (Baltimore, Md.) Jul 2007 - 1713-21 p. digital

Publication Type: Journal Article

0888-8809

10.1210/me.2007-0040 doi


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