The ambiguous role of NKX2-5 mutations in thyroid dysgenesis. [electronic resource]

By:

van Engelen, Klaartje

Contributor(s):

Mommersteeg, Mathilda T M
Baars, Marieke J H
Lam, Jan
Ilgun, Aho
van Trotsenburg, A S Paul
Smets, Anne M J B
Christoffels, Vincent M
Mulder, Barbara J M
Postma, Alex V

Producer: 20130627Description: e52685 p. digitalISSN:

1932-6203

Subject(s):

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

Online resources:

Available from publisher's website

In: PloS one vol. 7

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

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

APA

van Engelen K., Mommersteeg M. T. M., Baars M. J. H., Lam J., Ilgun A., van Trotsenburg A. S. P., Smets A. M. J. B., Christoffels V. M., Mulder B. J. M. & Postma A. V. (20130627). The ambiguous role of NKX2-5 mutations in thyroid dysgenesis. : PloS one.

Chicago

van Engelen Klaartje, Mommersteeg Mathilda T M, Baars Marieke J H, Lam Jan, Ilgun Aho, van Trotsenburg A S Paul, Smets Anne M J B, Christoffels Vincent M, Mulder Barbara J M and Postma Alex V. 20130627. The ambiguous role of NKX2-5 mutations in thyroid dysgenesis. : PloS one.

Harvard

van Engelen K., Mommersteeg M. T. M., Baars M. J. H., Lam J., Ilgun A., van Trotsenburg A. S. P., Smets A. M. J. B., Christoffels V. M., Mulder B. J. M. and Postma A. V. (20130627). The ambiguous role of NKX2-5 mutations in thyroid dysgenesis. : PloS one.

MLA

van Engelen Klaartje, Mommersteeg Mathilda T M, Baars Marieke J H, Lam Jan, Ilgun Aho, van Trotsenburg A S Paul, Smets Anne M J B, Christoffels Vincent M, Mulder Barbara J M and Postma Alex V. The ambiguous role of NKX2-5 mutations in thyroid dysgenesis. : PloS one. 20130627.

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