Identification of <b><i>Transient Receptor Potential Channel 4-Associated Protein</i></b> as a Novel Candidate Gene Causing Congenital Primary Hypothyroidism-Reference-Cited by-同舟云学术

Identification of Transient Receptor Potential Channel 4-Associated Protein as a Novel Candidate Gene Causing Congenital Primary Hypothyroidism

Published:2020 Issue:1 Volume:93 Page:16-29
ISSN:1663-2818
Container-title:Hormone Research in Paediatrics
language:en
Short-container-title:Horm Res Paediatr

Author:

Choukair Daniela,Eberle Birgit,Vick Philipp^ORCID,Hermanns Pia,Weiss Birgit,Paramasivam Nagarajan,Schlesner Matthias,Lornsen Katharina,Roeth Ralph,Klutmann Carina,Kreis Jennifer,Hoffmann Georg F.,Pohlenz Joachim,Rappold Gudrun A.,Bettendorf Markus

Publisher

S. Karger AG

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism,Pediatrics, Perinatology and Child Health

Reference32 articles.

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4. Persani L, Rurale G, de Filippis T, Galazzi E, Muzza M, Fugazzola L. Genetics and management of congenital hypothyroidism. Best Pract Res Clin Endocrinol Metab. 2018 Aug;32(4):387–96.

5. Stoupa A, Adam F, Kariyawasam D, Strassel C, Gawade S, Szinnai G, et al. TUBB1 mutations cause thyroid dysgenesis associated with abnormal platelet physiology. EMBO Mol Med. 2018 Dec;10(12):e9569.

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