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Identification of PENDRIN ( SLC26A4 ) Mutations in Patients With Congenital Hypothyroidism and “Apparent” Thyroid Dysgenesis

✍ Scribed by Kühnen, Peter; Turan, Serap; Fröhler, Sebastian; Güran, Tülay; Abali, Saygin; Biebermann, Heike; Bereket, Abdullah; Grüters, Annette; Chen, Wei; Krude, Heiko

Book ID: 121376390
Publisher: Endocrine Society
Year: 2014
Tongue: English
Weight: 316 KB
Volume: 99
Category: Article
ISSN: 0021-972X
DOI: 10.1210/jc.2013-2619

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