The ambiguous role of NKX2-5 mutations in thyroid dysgenesis.

van Engelen, Klaartje

The ambiguous role of NKX2-5 mutations in thyroid dysgenesis. [electronic resource] - PloS one 2012 - e52685 p. digital

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

1932-6203

10.1371/journal.pone.0052685 doi


Adolescent
Adult
Aged
Aged, 80 and over
Amino Acid Sequence
Animals
Cell Nucleus--metabolism
Child
DNA-Binding Proteins--genetics
Female
Homeobox Protein Nkx-2.5
Homeodomain Proteins--genetics
Humans
Male
Middle Aged
Mutation
Pedigree
Phenotype
Promoter Regions, Genetic
Protein Transport
Sequence Alignment
Thyroid Dysgenesis--genetics
Transcription Factors--genetics
Transcriptional Activation
Young Adult